Novel compounds

ABSTRACT

Polypeptides and polynucleotides of the genes set forth in Table I and methods for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for utilizing polypeptides and polynucleotides of the genes set forth in Table I in diagnostic assays.

FIELD OF INVENTION

[0001] This invention relates to newly identified polypeptides and polynucleotides encoding such polypeptides, to their use in diagnosis and in identifying compounds that may be agonists, antagonists that are potentially useful in therapy, and to production of such polypeptides and polynucleotides. The polynucleotides and polypeptides of the present invention also relate to proteins with signal sequences which allow them to be secreted extracellularly or membrane-associated (hereinafter often referred collectively as secreted proteins or secreted polypeptides).

BACKGROUND OF THE INVENTION

[0002] The drug discovery process is currently undergoing a fundamental revolution as it embraces “functional genomics”, that is, high throughput genome- or gene-based biology. This approach as a means to identify genes and gene products as therapeutic targets is rapidly superseding earlier approaches based on- “positional cloning”. A phenotype, that is a biological function or genetic disease, would be identified and this would then be tracked back to the responsible gene, based on its genetic map position.

[0003] Functional genomics relies heavily on high-throughput DNA sequencing technologies and the various tools of bioinformatics to identify gene sequences of potential interest from the many molecular biology databases now available. There is a continuing need to identify and characterise further genes and their related polypeptides/proteins, as targets for drug discovery.

[0004] Proteins and polypeptides that are naturally secreted into blood, lymph and other body fluids, or secreted into the cellular membrane are of primary interest for pharmaceutical research and development. The reason for this interest is the relative ease to target protein therapeutics into their place of action (body fluids or the cellular membrane). The natural pathway for protein secretion into extracellular space is the endoplasmic reticulum in eukaryotes and the inner membrane in prokaryotes (Palade, 1975, Science, 189, 347; Milstein, Brownlee, Harrison, and Mathews, 1972, Nature New Biol., 239, 117; Blobel, and Dobberstein, 1975, J. Cell. Biol., 67, 835). On the other hand, there is no known natural pathway for exporting a protein from the exterior of the cells into the cytosol (with the exception of pinocytosis, a mechanism of snake venom toxin intrusion into cells). Therefore targeting protein therapeutics into cells poses extreme difficulties.

[0005] The secreted and membrane-associated proteins include but are not limited to all peptide hormones and their receptors (including but not limited to insulin, growth hormones, chemokines, cytokines, neuropeptides, integrins, kallikreins, lamins, melanins, natriuretic hormones, neuropsin, neurotropins, pituitiary hormones, pleiotropins, prostaglandins, secretogranins, selectins, thromboglobulins, thymosins), the breast and colon cancer gene products, leptin, the obesity gene protein and its receptors, serum albumin, superoxide dismutase, spliceosome proteins, 7TM (transmembrane) proteins also called as G-protein coupled receptors, immunoglobulins, several families of serine proteinases (including but not limited to proteins of the blood coagulation cascade, digestive enzymes), deoxyribonuclease I, etc.

[0006] Therapeutics based on secreted or membrane-associated proteins approved by FDA or foreign agencies include but are not limited to insulin, glucagon, growth hormone, chorionic gonadotropin, follicle stimulating hormone, luteinizing hormone, calcitonin, adrenocorticotropic hormone (ACTH), vasopressin, interleukines, interferones, immunoglobulins, lactoferrin (diverse products marketed by several companies), tissue-type plasminogen activator (Alteplase by Genentech), hyaulorindase (Wydase by Wyeth-Ayerst), dornase alpha (Pulmozyme\ by Genentech), Chymodiactin (chymopapain by Knoll), alglucerase (Ceredase by Genzyme), streptokinase (Kabikinase by Pharmacia) (Streptase by Astra), etc. This indicates that secreted and membrane-associated proteins have an established, proven history as therapeutic targets. Clearly, there is a need for identification and characterization of further secreted and membrane-associated proteins which can play a role in preventing, ameliorating or correcting dysfunction or disease, including but not limited to diabetes, breast-, prostate-, colon cancer and other malignant tumors, hyper- and hypotension, obesity, bulimia, anorexia, growth abnormalities, asthma, manic depression, dementia, delirium, mental retardation, Huntington's disease, Tourette's syndrome, schizophrenia, growth, mental or sexual development disorders, and dysfunctions of the blood cascade system including those leading to stroke. The proteins of the present invention which include the signal sequences are also useful to further elucidate the mechanism of protein transport which at present is not entirely understood, and thus can be used as research tools.

SUMMARY OF THE INVENTION

[0007] The present invention relates to particular polypeptides and polynucleotides of the genes set forth in Table I, including recombinant materials and methods for their production. Such polypeptides and polynucleotides are of interest in relation to methods of treatment of certain diseases, including, but not limited to, the diseases set forth in Tables III and V, hereinafter referred to as “diseases of the invention”. In a further aspect, the invention relates to methods for identifying agonists and antagonists (e.g., inhibitors) using the materials provided by the invention, and treating conditions associated with imbalance of polypeptides and/or polynucleotides of the genes set forth in Table I with the identified compounds. In still a further aspect, the invention relates to diagnostic assays for detecting diseases associated with inappropriate activity or levels the genes set forth in Table I. Another aspect of the invention concerns a polynucleotide comprising any of the nucleotide sequences set forth in the Sequence Listing and a polypeptide comprising a polypeptide encoded by the nucleotide sequence. In another aspect, the invention relates to a polypeptide comprising any of the polypeptide sequences set forth in the Sequence Listing and recombinant materials and methods for their production. Another aspect of the invention relates to methods for using such polypeptides and polynucleotides. Such uses include the treatment of diseases, abnormalities and disorders (hereinafter simply referred to as diseases) caused by abnormal expression, production, function and or metabolism of the genes of this invention, and such diseases are readily apparent by those skilled in the art from the homology to other proteins disclosed for each attached sequence. In still another aspect, the invention relates to methods to identify agonists and antagonists using the materials provided by the invention, and treating conditions associated with the imbalance with the identified compounds. Yet another aspect of the invention relates to diagnostic assays for detecting diseases associated with inappropriate activity or levels of the secreted proteins of the present invention.

DESCRIPTION OF THE INVENTION

[0008] In a first aspect, the present invention relates to polypeptides the genes set forth in Table I. Such polypeptides include:

[0009] (a) an isolated polypeptide encoded by a polynucleotide comprising a sequence set forth in the Sequence Listing, herein when referring to polynucleotides or polypeptides of the Sequence Listing, a reference is also made to the Sequence Listing referred to in the Sequence Listing;

[0010] (b) an isolated polypeptide comprising a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0011] (c) an isolated polypeptide comprising a polypeptide sequence set forth in the Sequence Listing;

[0012] (d) an isolated polypeptide having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0013] (e) a polypeptide sequence set forth in the Sequence Listing; and

[0014] (f) an isolated polypeptide having or comprising a polypeptide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polypeptide sequence set forth in the Sequence Listing;

[0015] (g) fragments and variants of such polypeptides in (a) to (f).

[0016] Polypeptides of the present invention are believed to be members of the gene families set forth in Table II. They are therefore of therapeutic and diagnostic interest for the reasons set forth in Tables III and V. The biological properties of the polypeptides and polynucleotides of the genes set forth in Table I are hereinafter referred to as “the biological activity” of polypeptides and polynucleotides of the genes set forth in Table I. Preferably, a polypeptide of the present invention exhibits at least one biological activity of the genes set forth in Table I.

[0017] Polypeptides of the present invention also include variants of the aforementioned polypeptides, including all allelic forms and splice variants. Such polypeptides vary from the reference polypeptide by insertions, deletions, and substitutions that may be conservative or non-conservative, or any combination thereof. Particularly preferred variants are those in which several, for instance from 50 to 30, from 30 to 20, from 20 to 10, from 10 to 5, from 5 to 3, from 3 to 2, from 2 to 1 or 1 amino acids are inserted, substituted, or deleted, in any combination.

[0018] Preferred fragments of polypeptides of the present invention include an isolated polypeptide comprising an amino acid sequence having at least 30, 50 or 100 contiguous amino acids from an amino acid sequence set forth in the Sequence Listing, or an isolated polypeptide comprising an amino acid sequence having at least 30, 50 or 100 contiguous amino acids truncated or deleted from an amino acid sequence set forth in the Sequence Listing. Preferred fragments are biologically active fragments that mediate the biological activity of polypeptides and polynucleotides of the genes set forth in Table I, including those with a similar activity or an improved activity, or with a decreased undesirable activity. Also preferred are those fragments that are antigenic or immunogenic in an animal, especially in a human.

[0019] Fragments of a polypeptide of the invention may be employed for producing the corresponding full-length polypeptide by peptide synthesis; therefore, these variants may be employed as intermediates for producing the full-length polypeptides of the invention. A polypeptide of the present invention may be in the form of the “mature” protein or may be a part of a larger protein such as a precursor or a fusion protein. It is often advantageous to include an additional amino acid sequence that contains secretory or leader sequences, pro-sequences, sequences that aid in purification, for instance multiple histidine residues, or an additional sequence for stability during recombinant production.

[0020] Polypeptides of the present invention can be prepared in any suitable manner, for instance by isolation form naturally occurring sources, from genetically engineered host cells comprising expression systems (vide infra) or by chemical synthesis, using for instance automated peptide synthesizers, or a combination of such methods. Means for preparing such polypeptides are well understood in the art.

[0021] In a further aspect, the present invention relates to polynucleotides of the genes set forth in Table I. Such polynucleotides include:

[0022] (a) an isolated polynucleotide comprising a polynucleotide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polynucleotide sequence set forth in the Sequence Listing;

[0023] (b) an isolated polynucleotide comprising a polynucleotide set forth in the Sequence Listing;

[0024] (c) an isolated polynucleotide having at least 95%, 96%, 97%, 98%, or 99% identity to a polynucleotide set forth in the Sequence Listing;

[0025] (d) an isolated polynucleotide set forth in the Sequence Listing;

[0026] (e) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0027] (f) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide set forth in the Sequence Listing;

[0028] (g) an isolated polynucleotide having a polynucleotide sequence encoding a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0029] (h) an isolated polynucleotide encoding a polypeptide set forth in the Sequence Listing;

[0030] (i) an isolated polynucleotide having or comprising a polynucleotide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polynucleotide sequence set forth in the Sequence Listing;

[0031] (j) an isolated polynucleotide having or comprising a polynucleotide sequence encoding a polypeptide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polypeptide sequence set forth in the Sequence Listing; and polynucleotides that are fragments and variants of the above mentioned polynucleotides or that are complementary to above mentioned polynucleotides, over the entire length thereof.

[0032] Preferred fragments of polynucleotides of the present invention include an isolated polynucleotide comprising an nucleotide sequence having at least 15, 30, 50 or 100 contiguous nucleotides from a sequence set forth in the Sequence Listing, or an isolated polynucleotide comprising a sequence having at least 30, 50 or 100 contiguous nucleotides truncated or deleted from a sequence set forth in the Sequence Listing.

[0033] Preferred variants of polynucleotides of the present invention include splice variants, allelic variants, and polymorphisms, including polynucleotides having one or more single nucleotide polymorphisms (SNPs).

[0034] Polynucleotides of the present invention also include polynucleotides encoding polypeptide variants that comprise an amino acid sequence set forth in the Sequence Listing and in which several, for instance from 50 to 30, from 30 to 20, from 20 to 10, from 10 to 5, from 5 to 3, from 3 to 2, from 2 to 1 or 1 amino acid residues are substituted, deleted or added, in any combination.

[0035] In a further aspect, the present invention provides polynucleotides that are RNA transcripts of the DNA sequences of the present invention. Accordingly, there is provided an RNA polynucleotide that:

[0036] (a) comprises an RNA transcript of the DNA sequence encoding a polypeptide set forth in the Sequence Listing;

[0037] (b) is a RNA transcript of a DNA sequence encoding a polypeptide set forth in the Sequence Listing;

[0038] (c) comprises an RNA transcript of a DNA sequence set forth in the Sequence Listing; or

[0039] (d) is a RNA transcript of a DNA sequence set forth in the Sequence Listing; and RNA polynucleotides that are complementary thereto.

[0040] The polynucleotide sequences set forth in the Sequence Listing show homology with the polynucleotide sequences set forth in Table II. A polynucleotide sequence set forth in the Sequence Listing is a cDNA sequence that encodes a polypeptide set forth in the Sequence Listing. A polynucleotide sequence encoding a polypeptide set forth in the Sequence Listing may be identical to a polypeptide encoding a sequence set forth in the Sequence Listing or it may be a sequence other than a sequence set forth in the Sequence Listing, which, as a result of the redundancy (degeneracy) of the genetic code, also encodes a polypeptide set forth in the Sequence Listing. A polypeptide of a sequence set forth in the Sequence Listing is related to other proteins of the gene families set forth in Table II, having homology and/or structural similarity with the polypeptides set forth in Table II. Preferred polypeptides and polynucleotides of the present invention are expected to have, inter alia, similar biological functions/properties to their homologous polypeptides and polynucleotides. Furthermore, preferred polypeptides and polynucleotides of the present invention have at least one activity of the genes set forth in Table I.

[0041] Polynucleotides of the present invention may be obtained using standard cloning and screening techniques from a cDNA library derived from mRNA from the tissues set forth in Table IV (see for instance, Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)). Polynucleotides of the invention can also be obtained from natural sources such as genomic DNA libraries or can be synthesized using well known and commercially available techniques.

[0042] When polynucleotides of the present invention are used for the recombinant production of polypeptides of the present invention, the polynucleotide may include the coding sequence for the mature polypeptide, by itself, or the coding sequence for the mature polypeptide in reading frame with other coding sequences, such as those encoding a leader or secretory sequence, a pre-, or pro- or prepro- protein sequence, or other fusion peptide portions. For example, a marker sequence that facilitates purification of the fused polypeptide can be encoded. In certain preferred embodiments of this aspect of the invention, the marker sequence is a hexa-histidine peptide, as provided in the pQE vector (Qiagen, Inc.) and described in Gentz et al., Proc Natl Acad Sci USA (1989) 86:821-824, or is an HA tag. A polynucleotide may also contain non-coding 5′ and 3′ sequences, such as transcribed, non-translated sequences, splicing and polyadenylation signals, ribosome binding sites and sequences that stabilize mRNA.

[0043] Polynucleotides that are identical, or have sufficient identity to a polynucleotide sequence set forth in the Sequence Listing, may be used as hybridization probes for cDNA and genomic DNA or as primers for a nucleic acid amplification reaction (for instance, PCR). Such probes and primers may be used to isolate full-length cDNAs and genomic clones encoding polypeptides of the present invention and to isolate cDNA and genoric clones of other genes (including genes encoding paralogs from human sources and orthologs and paralogs from species other than) that have a high sequence similarity to sequences set forth in the Sequence Listing, typically at least 95% identity. Preferred probes and primers will generally comprise at least 15 nucleotides, preferably, at least 30 nucleotides and may have at least 50, if not at least 100 nucleotides. Particularly preferred probes will have between 30 and 50 nucleotides. Particularly preferred primers will have between 20 and 25 nucleotides.

[0044] A polynucleotide encoding a polypeptide of the present invention, including homologs from species other than, may be obtained by a process comprising the steps of screening a library under stringent hybridization conditions with a labeled probe having a sequence set forth in the Sequence Listing or a fragment thereof, preferably of at least 15 nucleotides; and isolating full-length cDNA and genomic clones containing the polynucleotide sequence set forth in the Sequence Listing. Such hybridization techniques are well known to the skilled artisan. Preferred stringent hybridization conditions include overnight incubation at 42° C. in a solution comprising: 50% formamide, 5×SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5× Denhardt's solution, 10% dextran sulfate, and 20 microgram/ml denatured, sheared salmon sperm DNA; followed by washing the filters in 0.1×SSC at about 65° C. Thus the present invention also includes isolated polynucleotides, preferably with a nucleotide sequence of at least 100, obtained by screening a library under stringent hybridization conditions with a labeled probe having the sequence set forth in the Sequence Listing or a fragment thereof, preferably of at least 15 nucleotides.

[0045] The skilled artisan will appreciate that, in many cases, an isolated cDNA sequence will be incomplete, in that the region coding for the polypeptide does not extend all the way through to the 5′terminus. This is a consequence of reverse transcriptase, an enzyme with inherently low “processivity” (a measure of the ability of the enzyme to remain attached to the template during the polymerisation reaction), failing to complete a DNA copy of the mRNA template during first strand cDNA synthesis.

[0046] There are several methods available and well known to those skilled in the art to obtain full-length cDNAs, or extend short cDNAs, for example those based on the method of Rapid Amplification of cDNA ends (RACE) (see, for example, Frohman et al., Proc Nat Acad Sci USA 85, 8998-9002, 1988). Recent modifications of the technique, exemplified by the Marathon (trade mark) technology (Clontech Laboratories Inc.) for example, have significantly simplified the search for longer cDNAs. In the Marathon (trade mark) technology, cDNAs have been prepared from mRNA extracted from a chosen tissue and an ‘adaptor’ sequence ligated onto each end. Nucleic acid amplification (PCR) is then carried out to amplify the “missing” 5′ end of the cDNA using a combination of gene specific and adaptor specific oligonucleotide primers. The PCR reaction is then repeated using ‘nested’ primers, that is, primers designed to anneal within the amplified product (typically an adapter specific primer that anneals further 3′ in the adaptor sequence and a gene specific primer that anneals further 5′ in the known gene sequence). The products of this reaction can then be analyzed by DNA sequencing and a full-length cDNA constructed either by joining the product directly to the existing cDNA to give a complete sequence, or carrying out a separate full-length PCR using the new sequence information for the design of the 5′ primer.

[0047] Recombinant polypeptides of the present invention may be prepared by processes well known in the art from genetically engineered host cells comprising expression systems. Accordingly, in a further aspect, the present invention relates to expression systems comprising a polynucleotide or polynucleotides of the present invention, to host cells which are genetically engineered with such expression systems and to the production of polypeptides of the invention by recombinant techniques. Cell-free translation systems can also be employed to produce such proteins using RNAs derived from the DNA constructs of the present invention.

[0048] For recombinant production, host cells can be genetically engineered to incorporate expression systems or portions thereof for polynucleotides of the present invention. Polynucleotides may be introduced into host cells by methods described in many standard laboratory manuals, such as Davis et al., Basic Methods in Molecular Biology (1986) and Sambrook et al. (ibid). Preferred methods of introducing polynucleotides into host cells include, for instance, calcium phosphate transfection, DEAE-dextran mediated transfection, transvection, micro-injection, cationic lipid-mediated transfection, electroporation, transduction, scrape loading, ballistic introduction or infection.

[0049] Representative examples of appropriate hosts include bacterial cells, such as Streptococci, Staphylococci, E. coli, Streptomyces and Bacillus subtilis cells; fungal cells, such as yeast cells and Aspergillus cells; insect cells such as Drosophila S2 and Spodoptera Sf9 cells; animal cells such as CHO, COS, HeLa, C127, 3T3, BHK, HEK 293 and Bowes melanoma cells; and plant cells.

[0050] A great variety of expression systems can be used, for instance, chromosomal, episomal and virus-derived systems, e.g., vectors derived from bacterial plasmids, from bacteriophage, from transposons, from yeast episomes, from insertion elements, from yeast chromosomal elements, from viruses such as baculoviruses, papova viruses, such as SV40, vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabies viruses and retroviruses, and vectors derived from combinations thereof, such as those derived from plasmid and bacteriophage genetic elements, such as cosmids and phagemids. The expression systems may contain control regions that regulate as well as engender expression. Generally, any system or vector that is able to maintain, propagate or express a polynucleotide to produce a polypeptide in a host may be used. The appropriate polynucleotide sequence may be inserted into an expression system by any of a variety of well-known and routine techniques, such as, for example, those set forth in Sambrook et al., (ibid). Appropriate secretion signals may be incorporated into the desired polypeptide to allow secretion of the translated protein into the lumen of the endoplasmic reticulum, the periplasmic space or the extracellular environment. These signals may be endogenous to the polypeptide or they may be heterologous signals.

[0051] If a polypeptide of the present invention is to be expressed for use in screening assays, it is generally preferred that the polypeptide be produced at the surface of the cell. In this event, the cells may be harvested prior to use in the screening assay. If the polypeptide is secreted into the medium, the medium can be recovered in order to recover and purify the polypeptide. If produced intracellularly, the cells must first be lysed before the polypeptide is recovered.

[0052] Polypeptides of the present invention can be recovered and purified from recombinant cell cultures by well-known methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Most preferably, high performance liquid chromatography is employed for purification. Well known techniques for refolding proteins may be employed to regenerate active conformation when the polypeptide is denatured during intracellular synthesis, isolation and/or purification.

[0053] Polynucleotides of the present invention may be used as diagnostic reagents, through detecting mutations in the associated gene. Detection of a mutated form of a gene is characterized by the polynucleotides set forth in the Sequence Listing in the cDNA or genomic sequence and which is associated with a dysfunction. Will provide a diagnostic tool that can add to, or define, a diagnosis of a disease, or susceptibility to a disease, which results from under-expression, overexpression or altered spatial or temporal expression of the gene. Individuals carrying mutations in the gene may be detected at the DNA level by a variety of techniques well known in the art.

[0054] Nucleic acids for diagnosis may be obtained from a subject's cells, such as from blood, urine, saliva, tissue biopsy or autopsy material. The genomic DNA may be used directly for detection or it may be amplified enzymatically by using PCR, preferably RT-PCR, or other amplification techniques prior to analysis. RNA or cDNA may also be used in similar fashion. Deletions and insertions can be detected by a change in size of the amplified product in comparison to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to labeled nucleotide sequences of the genes set forth in Table I. Perfectly matched sequences can be distinguished from mismatched duplexes by RNase digestion or by differences in melting temperatures. DNA sequence difference may also be detected by alterations in the electrophoretic mobility of DNA fragments in gels, with or without denaturing agents, or by direct DNA sequencing (see, for instance, Myers et al., Science (1985)230:1242). Sequence changes at specific locations may also be revealed by nuclease protection assays, such as RNase and S1 protection or the chemical cleavage method (see Cotton et al., Proc Natl Acad Sci USA (1985) 85: 4397-4401).

[0055] An array of oligonucleotides probes comprising polynucleotide sequences or fragments thereof of the genes set forth in Table I can be constructed to conduct efficient screening of e.g., genetic mutations. Such arrays are preferably high density arrays or grids. Array technology methods are well known and have general applicability and can be used to address a variety of questions in molecular genetics including gene expression, genetic linkage, and genetic variability, see, for example, M. Chee et al., Science, 274, 610-613 (1996) and other references cited therein.

[0056] Detection of abnormally decreased or increased levels of polypeptide or mRNA expression may also be used for diagnosing or determining susceptibility of a subject to a disease of the invention. Decreased or increased expression can be measured at the RNA level using any of the methods well known in the art for the quantitation of polynucleotides, such as, for example, nucleic acid amplification, for instance PCR, RT-PCR, RNase protection, Northern blotting and other hybridization methods. Assay techniques that can be used to determine levels of a protein, such as a polypeptide of the present invention, in a sample derived from a host are well-known to those of skill in the art. Such assay methods include radio-immunoassays, competitive-binding assays, Western Blot analysis and ELISA assays.

[0057] Thus in another aspect, the present invention relates to a diagnostic kit comprising:

[0058] (a) a polynucleotide of the present invention, preferably the nucleotide sequence set forth in the Sequence Listing, or a fragment or an RNA transcript thereof;

[0059] (b) a nucleotide sequence complementary to that of (a);

[0060] (c) a polypeptide of the present invention, preferably the polypeptide set forth in the Sequence Listing or a fragment thereof; or

[0061] (d) an antibody to a polypeptide of the present invention, preferably to the polypeptide set forth in the Sequence Listing.

[0062] It will be appreciated that in any such kit, (a), (b), (c) or (d) may comprise a substantial component. Such a kit will be of use in diagnosing a disease or susceptibility to a disease, particularly diseases of the invention, amongst others.

[0063] The polynucleotide sequences of the present invention are valuable for chromosome localisation studies. The sequences set forth in the Sequence Listing are specifically targeted to, and can hybridize with, a particular location on an individual human chromosome. The mapping of relevant sequences to chromosomes according to the present invention is an important first step in correlating those sequences with gene associated disease. Once a sequence has been mapped to a precise chromosomal location, the physical position of the sequence on the chromosome can be correlated with genetic map data. Such data are found in, for example, V. McKusick, Mendelian Inheritance in Man (available on-line through Johns Hopkins University Welch Medical Library). The relationship between genes and diseases that have been mapped to the same chromosomal region are then identified through linkage analysis (co-inheritance of physically adjacent genes). Precise human chromosomal localisations for a genomic sequence (gene fragment etc.) can be determined using Radiation Hybrid (RH) Mapping (Walter, M. Spillett, D., Thomas, P., Weissenbach, J., and Goodfellow, P., (1994) A method for constructing radiation hybrid maps of whole genomes, Nature Genetics 7, 22-28). A number of RH panels are available from Research Genetics (Huntsville, Ala., USA) e.g. the GeneBridge4 RH panel (Hum Mol Genet 1996 March;5(3):339-46 A radiation hybrid map of the human genome. Gyapay G, Schmitt K, Fizames C, Jones H, Vega-Czarny N, Spillett D, Muselet D, Prud′Homme J F, Dib C, Auffray C, Morissette J, Weissenbach J, Goodfellow P N). To determine the chromosomal location of a gene using this panel, 93 PCRs are performed using primers designed from the gene of interest on RH DNAs. Each of these DNAs contains random human genomic fragments maintained in a hamster background (human/hamster hybrid cell lines). These PCRs result in 93 scores indicating the presence or absence of the PCR product of the gene of interest. These scores are compared with scores created using PCR products from genomic sequences of known location. This comparison is conducted at http://www.genome.wi.mit.edu/.

[0064] The polynucleotide sequences of the present invention are also valuable tools for tissue expression studies. Such studies allow the determination of expression patterns of polynucleotides of the present invention which may give an indication as to the expression patterns of the encoded polypeptides in tissues, by detecting the mRNAs that encode them. The techniques used are well known in the art and include in situ hydridization techniques to clones arrayed on a grid, such as cDNA microarray hybridization (Schena et al, Science, 270, 467-470, 1995 and Shalon et al, Genome Res, 6, 639-645, 1996) and nucleotide amplification techniques such as PCR. A preferred method uses the TAQMAN (Trade mark) technology available from Perkin Elmer. Results from these studies can provide an indication of the normal function of the polypeptide in the organism. In addition, comparative studies of the normal expression pattern of mRNAs with that of mRNAs encoded by an alternative form of the same gene (for example, one having an alteration in polypeptide coding potential or a regulatory mutation) can provide valuable insights into the role of the polypeptides of the present invention, or that of inappropriate expression thereof in disease. Such inappropriate expression may be of a temporal, spatial or simply quantitative nature.

[0065] A further aspect of the present invention relates to antibodies. The polypeptides of the invention or their fragments, or cells expressing them, can be used as immunogens to produce antibodies that are immunospecific for polypeptides of the present invention. The term “immunospecific” means that the antibodies have substantially greater affinity for the polypeptides of the invention than their affinity for other related polypeptides in the prior art.

[0066] Antibodies generated against polypeptides of the present invention may be obtained by administering the polypeptides or epitope-bearing fragments, or cells to an animal, preferably a non-human animal, using routine protocols. For preparation of monoclonal antibodies, any technique which provides antibodies produced by continuous cell line cultures can be used. Examples include the hybridoma technique (Kohler, G. and Milstein, C., Nature (1975) 256:495-497), the trioma technique, the human B-cell hybridoma technique (Kozbor et al., Immunology Today (1983) 4:72) and the EBV-hybridoma technique (Cole et al., Monoclonal Antibodies and Cancer Therapy, 77-96, Alan R. Liss, Inc., 1985).

[0067] Techniques for the production of single chain antibodies, such as those described in U.S. Pat. No. 4,946,778, can also be adapted to produce single chain antibodies to polypeptides of this invention. Also, transgenic mice, or other organisms, including other mammals, may be used to express humanized antibodies.

[0068] The above-described antibodies may be employed to isolate or to identify clones expressing the polypeptide or to purify the polypeptides by affinity chromatography. Antibodies against polypeptides of the present invention may also be employed to treat diseases of the invention, amongst others.

[0069] Polypeptides and polynucleotides of the present invention may also be used as vaccines. Accordingly, in a further aspect, the present invention relates to a method for inducing an immunological response in a mammal that comprises inoculating the mammal with a polypeptide of the present invention, adequate to produce antibody and/or T cell immune response, including, for example, cytokine-producing T cells or cytotoxic T cells, to protect said animal from disease, whether that disease is already established within the individual or not. An immunological response in a mammal may also be induced by a method comprises delivering a polypeptide of the present invention via a vector directing expression of the polynucleotide and coding for the polypeptide in vivo in order to induce such an immunological response to produce antibody to protect said animal from diseases of the invention. One way of administering the vector is by accelerating it into the desired cells as a coating on particles or otherwise. Such nucleic acid vector may comprise DNA, RNA, a modified nucleic acid, or a DNA/RNA hybrid. For use a vaccine, a polypeptide or a nucleic acid vector will be normally provided as a vaccine formulation (composition). The formulation may further comprise a suitable carrier. Since a polypeptide may be broken down in the stomach, it is preferably administered parenterally (for instance, subcutaneous, intra-muscular, intravenous, or intra-dermal injection). Formulations suitable for parenteral administration include aqueous and non-aqueous sterile injection solutions that may contain anti-oxidants, buffers, bacteriostats and solutes that render the formulation instonic with the blood of the recipient; and aqueous and non-aqueous sterile suspensions that may include suspending agents or thickening agents. The formulations may be presented in unit-dose or multi-dose containers, for example, sealed ampoules and vials and may be stored in a freeze-dried condition requiring only the addition of the sterile liquid carrier immediately prior to use. The vaccine formulation may also include adjuvant systems for enhancing the immunogenicity of the formulation, such as oil-in water systems and other systems known in the art. The dosage will depend on the specific activity of the vaccine and can be readily determined by routine experimentation.

[0070] Polypeptides of the present invention have one or more biological functions that are of relevance in one or more disease states, in particular the diseases of the invention hereinbefore mentioned. It is therefore useful to identify compounds that stimulate or inhibit the function or level of the polypeptide. Accordingly, in a further aspect, the present invention provides for a method of screening compounds to identify those that stimulate or inhibit the function or level of the polypeptide. Such methods identify agonists or antagonists that may be employed for therapeutic and prophylactic purposes for such diseases of the invention as hereinbefore mentioned. Compounds may be identified from a variety of sources, for example, cells, cell-free preparations, chemical libraries, collections of chemical compounds, and natural product mixtures. Such agonists or antagonists so-identified may be natural or modified substrates, ligands, receptors, enzymes, etc., as the case may be, of the polypeptide; a structural or functional mimetic thereof (see Coligan et al., Current Protocols in Immunology 1(2):Chapter 5 (1991)) or a small molecule. Such small molecules preferably have a molecular weight below 2,000 daltons, more preferably between 300 and 1,000 daltons, and most preferably between 400 and 700 daltons. It is preferred that these small molecules are organic molecules.

[0071] The screening method may simply measure the binding of a candidate compound to the polypeptide, or to cells or membranes bearing the polypeptide, or a fusion protein thereof, by means of a label directly or indirectly associated with the candidate compound. Alternatively, the screening method may involve measuring or detecting (qualitatively or quantitatively) the competitive binding of a candidate compound to the polypeptide against a labeled competitor (e.g. agonist or antagonist). Further, these screening methods may test whether the candidate compound results in a signal generated by activation or inhibition of the polypeptide, using detection systems appropriate to the cells bearing the polypeptide. Inhibitors of activation are generally assayed in the presence of a known agonist and the effect on activation by the agonist by the presence of the candidate compound is observed. Further, the screening methods may simply comprise the steps of mixing a candidate compound with a solution containing a polypeptide of the present invention, to form a mixture, measuring an activity of the genes set forth in Table I in the mixture, and comparing activity of the mixture of the genes set forth in Table I to a control mixture which contains no candidate compound.

[0072] Polypeptides of the present invention may be employed in conventional low capacity screening methods and also in high-throughput screening (HTS) formats. Such HTS formats include not only the well-established use of 96- and, more recently, 384-well micotiter plates but also emerging methods such as the nanowell method described by Schullek et al, Anal Biochem., 246, 20-29, (1997).

[0073] Fusion proteins, such as those made from Fc portion and polypeptide of the genes set forth in Table I, as hereinbefore described, can also be used for high-throughput screening assays to identify antagonists for the polypeptide of the present invention (see D. Bennett et al., J Mol Recognition, 8:52-58 (1995); and K. Johanson et al., J Biol Chem, 270(16):9459-9471 (1995)).

[0074] The polynucleotides, polypeptides and antibodies to the polypeptide of the present invention may also be used to configure screening methods for detecting the effect of added compounds on the production of mRNA and polypeptide in cells. For example, an ELISA assay may be constructed for measuring secreted or cell associated levels of polypeptide using monoclonal and polyclonal antibodies by standard methods known in the art. This can be used to discover agents that may inhibit or enhance the production of polypeptide (also called antagonist or agonist, respectively) from suitably manipulated cells or tissues.

[0075] A polypeptide of the present invention may be used to identify membrane bound or soluble receptors, if any, through standard receptor binding techniques known in the art. These include, but are not limited to, ligand binding and crosslinking assays in which the polypeptide is labeled with a radioactive isotope (for instance, ¹²⁵I), chemically modified (for instance, biotinylated), or fused to a peptide sequence suitable for detection or purification, and incubated with a source of the putative receptor (cells, cell membranes, cell supernatants, tissue extracts, bodily fluids). Other methods include biophysical techniques such as surface plasmon resonance and spectroscopy. These screening methods may also be used to identify agonists and antagonists of the polypeptide that compete with the binding of the polypeptide to its receptors, if any. Standard methods for conducting such assays are well understood in the art.

[0076] Examples of antagonists of polypeptides of the present invention include antibodies or, in some cases, oligonucleotides or proteins that are closely related to the ligands, substrates, receptors, enzymes, etc., as the case may be, of the polypeptide, e.g., a fragment of the ligands, substrates, receptors, enzymes, etc.; or a small molecule that bind to the polypeptide of the present invention but do not elicit a response, so that the activity of the polypeptide is prevented.

[0077] Screening methods may also involve the use of transgenic technology and the genes set forth in Table I. The art of constructing transgenic animals is well established. For example, the genes set forth in Table I may be introduced through microinjection into the male pronucleus of fertilized oocytes, retroviral transfer into pre- or post-implantation embryos, or injection of genetically modified, such as by electroporation, embryonic stem cells into host blastocysts. Particularly useful transgenic animals are so-called “knock-in” animals in which an animal gene is replaced by the human equivalent within the genome of that animal. Knock-in transgenic animals are useful in the drug discovery process, for target validation, where the compound is specific for the human target. Other useful transgenic animals are so-called “knock-out” animals in which the expression of the animal ortholog of a polypeptide of the present invention and encoded by an endogenous DNA sequence in a cell is partially or completely annulled. The gene knock-out may be targeted to specific cells or tissues, may occur only in certain cells or tissues as a consequence of the limitations of the technology, or may occur in all, or substantially all, cells in the animal. Transgenic animal technology also offers a whole animal expression cloning system in which introduced genes are expressed to give large amounts of polypeptides of the present invention

[0078] Screening kits for use in the above described methods form a further aspect of the present invention. Such screening kits comprise:

[0079] (a) a polypeptide of the present invention;

[0080] (b) a recombinant cell expressing a polypeptide of the present invention;

[0081] (c) a cell membrane expressing a polypeptide of the present invention; or

[0082] (d) an antibody to a polypeptide of the present invention; which polypeptide is preferably that set forth in the Sequence Listing.

[0083] It will be appreciated that in any such kit, (a), (b), (c) or (d) may comprise a substantial component.

[0084] Glossary

[0085] The following definitions are provided to facilitate understanding of certain terms used frequently hereinbefore.

[0086] “Antibodies” as used herein includes polyclonal and monoclonal antibodies, chimeric, single chain, and humanized antibodies, as well as Fab fragments, including the products of an Fab or other immunoglobulin expression library.

[0087] “Isolated” means altered “by the hand of man” from its natural state, i.e., if it occurs in nature, it has been changed or removed from its original environment, or both. For example, a polynucleotide or a polypeptide naturally present in a living organism is not “isolated,” but the same polynucleotide or polypeptide separated from the coexisting materials of its natural state is “isolated”, as the term is employed herein. Moreover, a polynucleotide or polypeptide that is introduced into an organism by transformation, genetic manipulation or by any other recombinant method is “isolated” even if it is still present in said organism, which organism may be living or non-living.

[0088] “Secreted protein activity or secreted polypeptide activity” or “biological activity of the secreted protein or secreted polypeptide” refers to the metabolic or physiologic function of said secreted protein including similar activities or improved activities or these activities with decreased undesirable side-effects. Also included are antigenic and immunogenic activities of said secreted protein.

[0089] “Secreted protein gene” refers to a polynucleotide comprising any of the attached nucleotide sequences or allelic variants thereof and/or their complements.

[0090] “Polynucleotide” generally refers to any polyribonucleotide (RNA) or polydeoxribonucleotide (DNA), which may be unmodified or modified RNA or DNA. “Polynucleotides” include, without limitation, single- and double-stranded DNA, DNA that is a mixture of single- and double-stranded regions, single- and double-stranded RNA, and RNA that is mixture of single- and double-stranded regions, hybrid molecules comprising DNA and RNA that may be single-stranded or, more typically, double-stranded or a mixture of single- and double-stranded regions. In addition, “polynucleotide” refers to triple-stranded regions comprising RNA or DNA or both RNA and DNA. The term “polynucleotide” also includes DNAs or RNAs containing one or more modified bases and DNAs or RNAs with backbones modified for stability or for other reasons. “Modified” bases include, for example, tritylated bases and unusual bases such as inosine. A variety of modifications may be made to DNA and RNA; thus, “polynucleotide” embraces chemically, enzymatically or metabolically modified forms of polynucleotides as typically found in nature, as well as the chemical forms of DNA and RNA characteristic of viruses and cells. “Polynucleotide” also embraces relatively short polynucleotides, often referred to as oligonucleotides.

[0091] “Polypeptide” refers to any polypeptide comprising two or more amino acids joined to each other by peptide bonds or modified peptide bonds, i.e., peptide isosteres. “Polypeptide” refers to both short chains, commonly referred to as peptides, oligopeptides or oligomers, and to longer chains, generally referred to as proteins. Polypeptides may contain amino acids other than the 20 gene-encoded amino acids. “Polypeptides” include amino acid sequences modified either by natural processes, such as post-translational processing, or by chemical modification techniques that are well known in the art. Such modifications are well described in basic texts and in more detailed monographs, as well as in a voluminous research literature. Modifications may occur anywhere in a polypeptide, including the peptide backbone, the amino acid side-chains and the amino or carboxyl termini. It will be appreciated that the same type of modification may be present to the same or varying degrees at several sites in a given polypeptide. Also, a given polypeptide may contain many types of modifications. Polypeptides may be branched as a result of ubiquitination, and they may be cyclic, with or without branching. Cyclic, branched and branched cyclic polypeptides may result from post-translation natural processes or may be made by synthetic methods. Modifications include acetylation, acylation, ADP-ribosylation, amidation, biotinylation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cystine, formation of pyroglutamate, formylation, gamma-carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination (see, for instance, Proteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York, 1993; Wold, F., Post-translational Protein Modifications: Perspectives and Prospects, 1-12, in Post-translational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York, 1983; Seifter et al., “Analysis for protein modifications and nonprotein cofactors”, Meth Enzymol, 182, 626-646, 1990, and Rattan et al., “Protein Synthesis: Post-translational Modifications and Aging”, Ann NY Acad Sci, 663, 48-62, 1992).

[0092] “Fragment” of a polypeptide sequence refers to a polypeptide sequence that is shorter than the reference sequence but that retains essentially the same biological function or activity as the reference polypeptide. “Fragment” of a polynucleotide sequence refers to a polynucleotide sequence that is shorter than the reference sequence set forth in the Sequence Listing.

[0093] “Variant” refers to a polynucleotide or polypeptide that differs from a reference polynucleotide or polypeptide, but retains the essential properties thereof. A typical variant of a polynucleotide differs in nucleotide sequence from the reference polynucleotide. Changes in the nucleotide sequence of the variant may or may not alter the amino acid sequence of a polypeptide encoded by the reference polynucleotide. Nucleotide changes may result in amino acid substitutions, additions, deletions, fusions and truncations in the polypeptide encoded by the reference sequence, as discussed below. A typical variant of a polypeptide differs in amino acid sequence from the reference polypeptide. Generally, alterations are limited so that the sequences of the reference polypeptide and the variant are closely similar overall and, in many regions, identical. A variant and reference polypeptide may differ in amino acid sequence by one or more substitutions, insertions, deletions in any combination. A substituted or inserted amino acid residue may or may not be one encoded by the genetic code. Typical conservative substitutions include Gly, Ala; Val, Ile, Leu; Asp, Glu; Asn, Gln; Ser, Thr; Lys, Arg; and Phe and Tyr. A variant of a polynucleotide or polypeptide may be naturally occurring such as an allele, or it may be a variant that is not known to occur naturally. Non-naturally occurring variants of polynucleotides and polypeptides may be made by mutagenesis techniques or by direct synthesis. Also included as variants are polypeptides having one or more post-translational modifications, for instance glycosylation, phosphorylation, methylation, ADP ribosylation and the like. Embodiments include methylation of the N-terminal amino acid, phosphorylations of serines and threonines and modification of C-terminal glycines.

[0094] “Allele” refers to one of two or more alternative forms of a gene occurring at a given locus in the genome.

[0095] “Polymorphism” refers to a variation in nucleotide sequence (and encoded polypeptide sequence, if relevant) at a given position in the genome within a population.

[0096] “Single Nucleotide Polymorphism” (SNP) refers to the occurrence of nucleotide variability at a single nucleotide position in the genome, within a population. An SNP may occur within a gene or within intergenic regions of the genome. SNPs can be assayed using Allele Specific Amplification (ASA). For the process at least 3 primers are required. A common primer is used in reverse complement to the polymorphism being assayed. This common primer can be between 50 and 1500 bps from the polymorphic base. The other two (or more) primers are identical to each other except that the final 3′base wobbles to match one of the two (or more) alleles that make up the polymorphism. Two (or more) PCR reactions are then conducted on sample DNA, each using the common primer and one of the Allele Specific Primers.

[0097] “Splice Variant” as used herein refers to cDNA molecules produced from RNA molecules initially transcribed from the same genomic DNA sequence but which have undergone alternative RNA splicing. Alternative RNA splicing occurs when a primary RNA transcript undergoes splicing, generally for the removal of introns, which results in the production of more than one mRNA molecule each of that may encode different amino acid sequences. The term splice variant also refers to the proteins encoded by the above cDNA molecules.

[0098] “Identity” reflects a relationship between two or more polypeptide sequences or two or more polynucleotide sequences, determined by comparing the sequences. In general, identity refers to an exact nucleotide to nucleotide or amino acid to amino acid correspondence of the two polynucleotide or two polypeptide sequences, respectively, over the length of the sequences being compared.

[0099] “% Identity”—For sequences where there is not an exact correspondence, a “% identity” may be determined. In general, the two sequences to be compared are aligned to give a maximum correlation between the sequences. This may include inserting “gaps” in either one or both sequences, to enhance the degree of alignment. A % identity may be determined over the whole length of each of the sequences being compared (so-called global alignment), that is particularly suitable for sequences of the same or very similar length, or over shorter, defined lengths (so-called local alignment), that is more suitable for sequences of unequal length.

[0100] “Similarity” is a further, more sophisticated measure of the relationship between two polypeptide sequences. In general, “similarity” means a comparison between the amino acids of two polypeptide chains, on a residue by residue basis, taking into account not only exact correspondences between a between pairs of residues, one from each of the sequences being compared (as for identity) but also, where there is not an exact correspondence, whether, on an evolutionary basis, one residue is a likely substitute for the other. This likelihood has an associated “score” from which the “% similarity” of the two sequences can then be determined.

[0101] Methods for comparing the identity and similarity of two or more sequences are well known in the art. Thus for instance, programs available in the Wisconsin Sequence Analysis Package, version 9.1 (Devereux J et al, Nucleic Acids Res, 12, 387-395, 1984, available from Genetics Computer Group, Madison, Wis., USA), for example the programs BESTFIT and GAP, may be used to determine the % identity between two polynucleotides and the % identity and the % similarity between two polypeptide sequences. BESTFIT uses the “local homology” algorithm of Smith and Waterman (J Mol Biol, 147,195-197, 1981, Advances in Applied Mathematics, 2, 482-489, 1981) and finds the best single region of similarity between two sequences. BESTFIT is more suited to comparing two polynucleotide or two polypeptide sequences that are dissimilar in length, the program assuming that the shorter sequence represents a portion of the longer. In comparison, GAP aligns two sequences, finding a “maximum similarity”, according to the algorithm of Neddleman and Wunsch (J Mol Biol, 48, 443-453, 1970). GAP is more suited to comparing sequences that are approximately the same length and an alignment is expected over the entire length. Preferably, the parameters “Gap Weight” and “Length Weight” used in each program are 50 and 3, for polynucleotide sequences and 12 and 4 for polypeptide sequences, respectively. Preferably, % identities and similarities are determined when the two sequences being compared are optimally aligned.

[0102] Other programs for determining identity and/or similarity between sequences are also known in the art, for instance the BLAST family of programs (Altschul S F et al, J Mol Biol, 215, 403-410, 1990, Altschul S F et al, Nucleic Acids Res., 25:389-3402, 1997, available from the National Center for Biotechnology Information (NCBI), Bethesda, Md., USA and accessible through the home page of the NCBI at www.ncbi.nlm.nih.gov) and FASTA (Pearson W R, Methods in Enzymology, 183, 63-99, 1990; Pearson W R and Lipman D J, Proc Nat Acad Sci USA, 85, 2444-2448,1988, available as part of the Wis. Sequence Analysis Package).

[0103] Preferably, the BLOSUM62 amino acid substitution matrix (Henikoff S and Henikoff J G, Proc. Nat. Acad Sci. USA, 89, 10915-10919, 1992) is used in polypeptide sequence comparisons including where nucleotide sequences are first translated into amino acid sequences before comparison.

[0104] Preferably, the program BESTFIT is used to determine the % identity of a query polynucleotide or a polypeptide sequence with respect to a reference polynucleotide or a polypeptide sequence, the query and the reference sequence being optimally aligned and the parameters of the program set at the default value, as hereinbefore described.

[0105] “Identity Index” is a measure of sequence relatedness which may be used to compare a candidate sequence (polynucleotide or polypeptide) and a reference sequence. Thus, for instance, a candidate polynucleotide sequence having, for example, an Identity Index of 0.95 compared to a reference polynucleotide sequence is identical to the reference sequence except that the candidate polynucleotide sequence may include on average up to five differences per each 100 nucleotides of the reference sequence. Such differences are selected from the group consisting of at least one nucleotide deletion, substitution, including transition and transversion, or insertion. These differences may occur at the 5′ or 3′ terminal positions of the reference polynucleotide sequence or anywhere between these terminal positions, interspersed either individually among the nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence. In other words, to obtain a polynucleotide sequence having an Identity Index of 0.95 compared to a reference polynucleotide sequence, an average of up to 5 in every 100 of the nucleotides of the in the reference sequence may be deleted, substituted or inserted, or any combination thereof, as hereinbefore described. The same applies mutatis mutandis for other values of the Identity Index, for instance 0.96, 0.97, 0.98 and 0.99.

[0106] Similarly, for a polypeptide, a candidate polypeptide sequence having, for example, an Identity Index of 0.95 compared to a reference polypeptide sequence is identical to the reference sequence except that the polypeptide sequence may include an average of up to five differences per each 100 amino acids of the reference sequence. Such differences are selected from the group consisting of at least one amino acid deletion, substitution, including conservative and non-conservative substitution, or insertion. These differences may occur at the amino- or carboxy-terminal positions of the reference polypeptide sequence or anywhere between these terminal positions, interspersed either individually among the amino acids in the reference sequence or in one or more contiguous groups within the reference sequence. In other words, to obtain a polypeptide sequence having an Identity Index of 0.95 compared to a reference polypeptide sequence, an average of up to 5 in every 100 of the amino acids in the reference sequence may be deleted, substituted or inserted, or any combination thereof, as hereinbefore described. The same applies mutatis mutandis for other values of the Identity Index, for instance 0.96, 0.97, 0.98 and 0.99.

[0107] The relationship between the number of nucleotide or amino acid differences and the Identity Index may be expressed in the following equation:

n _(a) ≦x _(a)−(x _(a) ·I),

[0108] in which:

[0109] n_(a) is the number of nucleotide or amino acid differences,

[0110] x_(a) is the total number of nucleotides or amino acids in a sequence set forth in the Sequence Listing,

[0111] I is the Identity Index,

[0112] · is the symbol for the multiplication operator, and in which any non-integer product of x_(a) and I is rounded down to the nearest integer prior to subtracting it from x_(a).

[0113] “Homolog” is a generic term used in the art to indicate a polynucleotide or polypeptide sequence possessing a high degree of sequence relatedness to a reference sequence. Such relatedness may be quantified by determining the degree of identity and/or similarity between the two sequences as hereinbefore defined. Falling within this generic term are the terms “ortholog”, and “paralog”. “Ortholog” refers to a polynucleotide or polypeptide that is the functional equivalent of the polynucleotide or polypeptide in another species. “Paralog” refers to a polynucleotideor polypeptide that within the same species which is functionally similar.

[0114] “Fusion protein” refers to a protein encoded by two, often unrelated, fused genes or fragments thereof. In one example, EP-A-0 464 533-A discloses fusion proteins comprising various portions of constant region of immunoglobulin molecules together with another human protein or part thereof. In many cases, employing an immunoglobulin Fc region as a part of a fusion protein is advantageous for use in therapy and diagnosis resulting in, for example, improved pharmacokinetic properties [see, e.g., EP-A 0232 262]. On the other hand, for some uses it would be desirable to be able to delete the Fc part after the fusion protein has been expressed, detected and purified.

[0115] All publications and references, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference in their entirety as if each individual publication or reference were specifically and individually indicated to be incorporated by reference herein as being fully set forth. Any patent application to which this application claims priority is also incorporated by reference herein in its entirety in the manner described above for publications and references. TABLE I Corresponding GSK Nucleic Acid Protein Gene Name Gene ID SEQ ID NO's SEQ ID NO's sbg101452SLITa 101452 SEQ ID NO: 1 SEQ ID NO: 27 sbg29046CYSa  29046a SEQ ID NO: 2 SEQ ID NO: 28 sbg29046CYSb  29046b SEQ ID NO: 3 SEQ ID NO: 29 SEQ ID NO: 4 SEQ ID NO: 30 sbg37149SLITb  37149 SEQ ID NO: 5 SEQ ID NO: 31 sbg36267SLIta  36267 SEQ ID NO: 6 SEQ ID NO: 32 sbg35579MELAa  35579 SEQ ID NO: 7 SEQ ID NO: 33 SEQ ID NO: 8 SEQ ID NO: 34 SBh69447.  69447 SEQ ID NO: 9 SEQ ID NO: 35 Triglyceride Lipase SBh86614.Tryp1  86614 SEQ ID NO: 10 SEQ ID NO: 36 SEQ ID NO: 11 SEQ ID NO: 37 sbg106886DELTAa 106886 SEQ ID NO: 12 SEQ ID NO: 38 sbg35779THYa  35779 SEQ ID NO: 13 SEQ ID NO: 39 sbg15130INHa  15130 SEQ ID NO: 14 SEQ ID NO: 40 SEQ ID NO: 15 SEQ ID NO: 41 SBh26548.homebox  26548 SEQ ID NO: 16 SEQ ID NO: 42 sbg26991CERUa  26991 SEQ ID NO: 17 SEQ ID NO: 43 sbg35851PEROa  35851 SEQ ID NO: 18 SEQ ID NO: 44 SEQ ID NO: 19 SEQ ID NO: 45 sbg36274SLITa  36274 SEQ ID NO: 20 SEQ ID NO: 46 sbg34575SLITa  34575 SEQ ID NO: 21 SEQ ID NO: 47 SBh71706.NIAP  71706 SEQ ID NO: 22 SEQ ID NO: 48 SEQ ID NO: 23 SEQ ID NO: 49 SBh77492.Breast  77492 SEQ ID NO: 24 SEQ ID NO: 50 Specific BS200 SEQ ID NO: 25 SEQ ID NO: 51 sbg115305LRRa 115305 SEQ ID NO: 26 SEQ ID NO: 52

[0116] TABLE II Closest Closest Cell Gene Polynuclotide by Polypeptide by Localization Gene Name Family homology homology (by homology) sbg101452SLITa Slit-like GB: AL138498 KIAA1246 Membrane- membrane Submitted (07-DEC-2000) protein,gi: 6330833 bound glycoprotein by Genoscope - Submitted (04-OCT-1999) Centre National de by Osamu Ohara, Kazusa Sequencage: BP 191 DNA Research Institute, 91006 EVRY cedex - Laboratory of DNA FRANCE Technology; 1532-3 Yana, Kisarazu, Chiba 292-0812, Japan sbg29046CYSa Cystatin GB: AL121894 Human cystatin family Secreted Submitted on Feb. member 18, 2000 by Sanger gi: 9944240 Centre, Hinxton, Submitted (25-OCT-2000) Cambridgeshire, CB10 Sanger Centre, Hinxton, ISA, UK Cambridgeshire, CB10 ISA, UK. sbg29046CYSb Cystatin GB: AL121894 Novel human cystatin- Secreted Submitted on Feb. related protein 18, 2000 by Sanger geneseqp: Y53771 Centre, Hinxton, (KARO-) KAROLINSKA Cambridgeshire, CB10 INNOVATIONS AB ISA, UK W09958565-A1, 18-NOV-99 sbg37149SLITb Slit-like GB: Z94160 Human putative leucine rich Membrane- membrane Submitted on Dec. 8, protein bound glycoprotein 1999, Sanger Centre, gi: 3191975 Hinxton, Submitted (08-DEC-1999) Cambridgeshire, CB10 Sanger Centre, Hinxton, ISA, UK. Cambridgeshire, CB10 ISA, UK. sbg36267SLIta Slit 3-like GB: AL080239 Human KIAA0918 protein, Membrane- membrane Submitted on Jan10, gi: 4240325 bound glycoprotein 2000, by Sanger Centre, Nagase, T., Ishikawa, K., Hinxton, Suyama, M., Kikuno, R., Cambridgeshire, CB10 Hirosawa, M., Miyajima, N., ISA, UK. Tanaka, A., Kotani, H., Nomura, N. and Ohara, O. DNA Res. 5 (6), 355-364 (1998) sbg35579MELAa Brain- GB: AC018477 Human KIAA1484 protein, Membrane- specific Submitted (12-DEC- gi: 7959229 bound transmembrane 1999) by Human Nagase, T., Kikuno, R., glycoprotein Genome Sequencing Ishikawa, K., Hirosawa, M. Center, Department of and Ohara, O. Molecular and Human DNA Res. 7 (2), 143-150 Genetics, Baylor College (2000). of Medicine, One Baylor Plaza, Houston, TX 77030, USA SBh69447. Triglyceride GB: AC011277 Human gastric lipase, Secreted Triglyceride lipase Submitted (05-OCT- gi: 4758676 Lipase 1999) by Whitehead Bodmer, M. W., Angal, S., Institute/MIT Center for Yarranton, G. T., Harris, T. J., Genome Research, 320 Lyons, A., King, D. J., Charles Street, Pieroni, G., Riviere, C., Cambridge, MA 02141, Verger, R. and Lowe, P. A. USA Biochim. Biophys. Acta 909 (3), 237-244 (1987) SBh86614.Tryp 1 Serine JGI: RPCI-11 ± Human PRO351 protein, Secreted protease 388M20 geneseqp: Y41704 Found at Joint Genome GENENTECH INC Institute WO9946281-A2, 16-SEP-99 sbg106886DELTAa DELTAa GB: AC021391 Rat preadipocyte factor, Secreted gi: 802014 Submitted on Carlsson, C., Tomehave, D., JAN 16, 2000, Whitehead Lindberg, K., Galante, P., Institute/MIT Center for Billestrup, N., Michelsen, B., Genome Research, 320 Larsson, L. I. and Nielsen, J. H. Charles Street, Endocrinology 138 (9), Cambridge, MA 02141, 3940-3948 (1997) USA sbg35779THYa Thyroxine GB: AL132990 Human PRO1337 Secreted binding Submitted (27-JAN- GENENTECH INC globulin 2000) by Genoscope - WO200012708-A2, 09- Centre National de MAR-00 Sequencage: BP 191 91006 EVRY cedex sbg15130INHa Leukocyte SC: Z93016 Human serine protease Secreted protease Submitted (31-JUL- inhibitor, geneseqp: Y28645 inhibitor 2000) Sanger Centre, Human Genome Sci Inc Hinxton, WO199940183-A1, 12- Cambridgeshire, CB10 AUG-99 ISA, UK. SBh26548. LBX, HOX, GB: AC005041 Mouse lady bird-like Nucleus homebox DLX Sulston, J. E. and homeobox 2 homolog, Waterston, R. gi: 6754512 Chen, F., Genome Res. 8 (11), Liu, K. C. and Epstein, J. A. 1097-1108 (1998) Mech. Dev. (1999). sbg26991CERUa Ceruloplasm GB: AC010909 Human ceruloplasmin, Secreted in precursor Submitted (26-SEP- gi: 1070458 Takahashi, N., 1999) by Whitehead Ortel, T. L. and Putnam, F. W. Institute/MIT Center for Proc. Natl. Acad. Sci. U.S.A. Genome Research, 320 81 (2), 390-394 (1984). Charles Street, Cambridge, MA 02141, USA sbg35851PEROa Slit-like GB: AF038458 Human KIAA1246 Membrane- membrane Submitted (12-DEC- protein,gi: 6330833 bound glycoprotein 1997) Human Genome Submitted (04-OCT-1999) Center, Lawrence by Osamu Ohara, Kazusa Livermore National DNA Research Institute, Laboratory, 7000 East Laboratory of DNA Ave., Livermore, CA Technology; 1532-3 Yana, 94551, USA Kisarazu, Chiba 292-0812, Japan sbg36274SLITa Slit-like GB: AL109653 Human novel protein, Membrane- membrane Submitted (22-NOV- gi: 11877257 Submitted bound glycoprotein 1999) Sanger Centre, (20-JAN-2000) Sanger Hinxton, Centre, Hinxton, Cambridgeshire, CB10 Cambridgeshire, CB10 ISA ISA, UK. sbg34575SLITa Slit-like GB: AC005343 pineal gland specific gene-1 Membrane- membrane Submitted (31-JUL- protein, geneseqp: W09405 bound glycoprotein 1998) by Molecular and Huaman Genome Sci Inc Human Genetics, Baylor WO9639158-A1, 12-DEC- College of Medicine, 96 One Baylor Plaza, Houston, TX 77030, USA. SBh71706.NIAP Apoptosis GB: AL121653 Human hypothetical protein, Cytosolic inhibitory Submission (29-FEB- weakly similar to mouse protein 2000) by Genoscope. neuronal apoptosis inhibitory protein 2, gi: 9367840 Submitted (15-JUL-2000) by Dept. Genetica Molecular, Institut de Recerca Oncologica (IRO), Hospital Duran i Reynals, Av. Gran Via s/n Km 2,7 L'Hospitalet de Llobregat, 08907 Barcelona, Catalunya, SPAIN. SBh77492.Breast EGF-related SC: Z82214,GB: Z99756 Mouse EGF-related protein Secreted Specific BS200 protein Submitted (08-DEC- SCUBEI, gi: 10998440 1999) by Sanger Centre, Submitted (08-JUN-2000) Hinxton, Mammalian Genetics Unit, Cambridgeshire, CB10 MRC Harwell, Chilton, ISA, UK. Didcot, Oxon OX11 0RD, United Kingdom. sbg115305LRRa Lucine-rich GB: AC023484 Muse leucine rich repeat Membrane- repeat Submitted (14-FEB- protein 1, gi: 678724 bound (LRR) 2000) Human Genomic Taguchi A, Wanaka A, Mori Center, Institute of T, Matsumoto K, Imai Y, Genetics, Chinese Tagaki T, Tohyama M, Academy of Sciences, 1996, Brain Res Mol Brain Datun Road, Beijing, Res;35: 31-4. Beijing 100101, P. R. China

[0117] TABLE III Gene Name Uses Associated Diseases sbg101452SLITa An embodiment of the invention is the use of Gastrointestinal ulceration, sbg101452SLITa, a member of the slit protein family,for Zollinger-Ellison syndrome, diagnosis and treatment of nervous and muscular diseases, congential microvillus atrophy, This is because other members of the slit protein family may skin diseases be necessary for CNS development. In addition, sbg101452SLITa shows homology to leucine-rich repeat proteins, which demonstrates siginificant functions in neural development. It is thus possible that similar molecules play a crucial role in the morphogenesis of the mammalian nervous system (Taniguchi H, Tohyama M, Takagi T. Brain Res Mol Brain Res 1996 Feb; 36(1): 45-52) sbg29046CYSa An embodiment of the invention is the use of sbg29046CYSa Cancer, infection, autoimmune to inhibit tumor formation and metastasis and may also be disorder, hematopoietic disorder, involved in natural tissue remodeling events such as bone wound healing, inflammation resorption and embryo implantation. Close Homologs of metastasis, amyloid sbg29046CYSa are cysteine protease inhibitors knows as angiopathies, and progressive cystatins. Cystatins and their target proteases have been myoclonus epilepsy associated with tumor formation and metastasis,but also are involved in natural tissue remodeling events such as bone resorption and embryo implantation (Tohonen V., Osterlund C., and Nordqvist K., 1998 Proc Natl Acad Sci USA 95(24): 14208-13). Cystatin is a natural and specific inhibitor of the cysteine proteases generating in cancer invasion. The level of cystatin determination in serum and tissue extracts can be the clinical diagnostic and prognostic parameters in human cancers (Kos J., Stabuc B., Cimerman N., and Brunner N., 1998. Clin Chem 44(12): 2556-7). sbg29046CYSb An embodiment of the invention is the use of sbg29046CYSb Cancer, infection, autoimmune to inhibit tumor formation and metastasis and may also be disorder, hematopoietic disorder, involved in natural tissue remodeling events such as bone wound healing, inflammation resorption and embryo implantation. Close homologs of metastasis, amyloid sbg29046CYSa are cysteine protease inhibitors known as angiopathies, and progressive cystatins. Cystatins and their target proteases have been myoclonus epilepsy associated with tumor formation and metastasis, but also are involved in natural tissue remodeling events such as bone resorption and embryo implantation (Tohonen V., Osterlund C., and Nordqvist K., 1998 Proc Natl Acad Sci USA 95(24): 14208-13). Cystatin is a natural and specific inhibitor of the cysteine Proteases generating in cancer invasion. The level of cystatin determination in serum and tissue extracts can be the clinical diagnostic and prognostic parameters in human cancer (Kos J., Stabuc B., Cimerman N., and Brunner N., 1998. Clin Chem 44(12): 2556-7). sbg37149SLITb An embodiment of the invention is the use of Cancer, infection, autoimmune sbg37149SLITb, amember of human slit-like proteins, disorder, hematopoietic disorder, which may be necessary for CNS development,and therefore would healing, inflammation, can be useful for diagnosis and treatment of nervous and and diseases in spinal cord, muscular diseases. In addition, sbg371495SLITb shows thyroid gland, ovary, prostate, similarity to leucine-rich repeat protiens,and may also renal gland, small intestine demonstrate significant function in neural developing. It heart, trachea, thymus, lymph has been shows that expression of slit genes is associated node, and muscular system with neuronal migration in the developing forebrain (HU H, Neuron 703-11,1999). Its is thus possible that sbg37149SLITb plays a crucial role in the morphogenesis of the mammalian nervous system (Taniguchi H, Tohyama M, Takagi T. Brain Res Mol Brain Res 1996 Feb; 36(1): 45-52) sbg36267SLITa An embodiment of the invention is the use of Gastrointestinal ulceration, sbg36267SLITa to treat gastrointestinal ulceration as well as diseases in spinal cord, thyroid prevention and treatment of diseases in spinal cord, thyroid gland, ovary, prostate, renal gland, ovary, prostate, renal gland, small intestine, heart, gland, small intestine, heart, trachea, thymus, lymph node, muscular system and colon. trachea, thymus, lymph node, sbg36267SLITa is exploitable in similar ways to a close muscular system and colon homolog human KIAA0918 protein, which is functionally related to cell signaling/communication, cell structure/motility and nucleic acid management. A close homolog of sbg36267SLITa is PRO266 and human slit 3 mature protein. sbg35579MELAa An embodiment of the invention is the use of Gastrointestinal ulceration, sbg35579MELAa diseases in spinal cord, thyroid The closest homologue to this novel protein is human gland, ovary, prostate, renal KIAA1484 protein which is derived from brain-specific gland, small intestine, heart, cDNA library and functionally related to cell trachea, thymus, lymph node, signaling/communication, cell structure/motility and nucleic muscular system and colon. acid management. Other close homologs to sbg35579MELAa are human KIAA1246, also derived from brain-specific cDNA library andhuman brain-specific transmembrane glycoprotein B09968. B09968 has a typical PDZ protein binding motif and functions as a cellular signal transducer, useful in developing drugs for treating nervous diseases SBh69447. An embodiment of the invention is the use of Cancer, infection, autoimmune Triglyceride SBh69447. Triglyceride Lipase, a member of gastric lipases, disorder, hematopoietic disorder, Lipase for oral administration to treat lipase deficiency in cystic wound healing, inflammation. fibrosis and pancreatitis. Some gastric lipases are also useful gastric lipase deficiency, cystic therapeutically for absorption of ingested fat in patients with fibrosis, Pancreatitis, altered mucoviscidioin of fat and defective transesterication absorption of fat, (WO8601532-A). gastrointestinal disorders, defective biocatalysis, mucoviscidosis, poor enymatic bioconversion of fat. cystic fibrosis, pncreatititis diseases SBh86614. Tryp1 An embodiment of the invention is the use of Cancer, infection, autoimmune SBh86614. Tryp1, a member of the mast cell protease/tryptase disorder, hematopoietic disorder, family, for treatment of undesirable clot formation wound healing disorder, such as myocardial infraction, during angioplasty and all inflammation, blood surgical procedures that require decreased blood clot coagulation disorders, cancers formation and may also be involved in tumor growth and and cellular adhesion disorders, fertility. Other homologs of the mast cell protease/ tryptase deep vein thrombosis, family have been identified in WO9836054-A1 and myocardial infraction WO9824886-A1. sbg106886 An embodiment of the invention is the use of Cancer, infection, autoimmune DELTAa sbg106886DELTAa in cellular interactions and fetal disorder, hematopoietic disorder, development. Close homologs of sbg106886DELTAa are wound healing, inflammation involved in cell-to-cell communications in mammalian embryos through the Notch signaling pathway, and therefore may have a role in cellular interactions (Artavanis-Tsakonas et al., 1995, Science 268: 225-232). It has been shown that mouse Delta1 protein is essential for normal somitogenesis and neuronal differentiation, and Delta1 expression can be detected during organogenesis and fetal development (Beckers J., Clark A., Wunsch K., Hrabe De Angelis M., Gossler A. 1999, Mech Dev 84: 165-8). sbg35779THYa An embodiment of the invention is the use of Thyroid and liver diseases, sbg35779THYa, a secreted protein, in the diagnosis and also septic shock, pancreatitis, in the treatment of thyroid and liver diseases, treatment of coagulation disorders, septic shock, pancreatitis, coagulation disorders, and microbial diseases microbial diseases. Close homologs of sbg35779THYa are Mutant Human alpha-1-antichymotrypsin with Arg(358) and Alpha-1-antichymotrypsin (Leu358Arg). sbg15130INHa An embodiment of the invention is the use of sbg15130INHa, Immune disorders, cancers, a secreted protein, in developing products for treating e.g. inflammation, transplant immune disorders, cancers, inflammation, transplant rejection rejection or infections, or infections. A close homolog of sbg 15130INHa is mouse disorders in fetal development and rat secretory leukocyte protease inhibitors (SLIPI). Transfection of macrophages with SLPI have been shown to suppress LPS-induced activation of NF-kappa B and production of nitric oxide and TNF alpha (Jin, F. Y., Nathan, C., Radzioch, D. and Ding, A. Cell 88 (3), 417-426 (1997). SBh26548. An embodiment of the invention is the use of SBh26548 Autoimmune disorder, home-box homebox to enhance bone thickness and increase bone hematopoietic disorder, wound density at the site of application or may affect developmental healing disorder, cancer, conditions if expressed in the thymus or T cells. Close inflammation, viral and homologs of SBh26548 homebox are members of HOX and bacterial infection, autosomal DLX (US5850002-A and WO9943784-A2). dominant disorder, bone defects, osteoperosis, trauma, peridontal defects sbg26991CERUa An embodiment of the invention is the use of Cancer, infection, autoimmune sbg26991CERUa to reduce the loss of essential ferroxidases. disorder, hematopoietic disorder, Copper is an essential trace metal which plays a fundamental wound healing disorder, role in the biochemistry of the human nervous system. Close inflammation, and progressive homologs of sbg26991CERUa are Ceruloplasmins. neurodegeneration of the retina Ceruloplasmins are plasma metalloproteins that contains 95% and basal ganglia of the copper found in human plasma and inherited loss of this essential ferroxidase is associated with progressive neurodegeneration of the retina and basal ganglia (Waggoner DJ, Bartnikas TB, Gitlin JD, 1999 Neurobiol Dis 6(4): 221-30. Ceruloplasmin deficiency leads to iron accumulation and causes damage to a variety of tissues and organs. Serum ceruloplamin determination can be part of diagnostic procedures of Wilson's disease, an inherited copper storage disease. sbg35851PEROa An embodiment of the invention is the use of Cancer, Gastrointestinal sbg35851PEROa, a member of the slit protein family, for ulceration, Zollinger-Ellison diagnosis and treatment of nervous and muscular diseases. In syndrome, congenital addition, sbg35851PEROa shows homologyto leucine-rich microvillus atrophy, skin repeat proteins, which demonstrates siginificant functions in diseases, diseases associated neural development. It is thus possible that similar molecules with nervous system. play a crucial role in the morphogenesis of the mammalian nervous system (Taniguchi H, Tohyama M, Takagi T. Brain Res Mol Brain Res 1996 Feb; 36(1): 45-52). sbg36274SLITa An embodiment of the invention is the use of Cancer, infection, autoimmune sbg36274SLITa, a member of human slit-like proteins, disorder, hematopoietic disorder, which may be necessary for CNS development, and therefore wound healing disorder, can be useful for diagnosis and treatment of nervous and inflammation, gastrointestinal muscular diseases. A close homolog of sbg36274SLITa is ulceration, and diseases in insulin-like growth factor. Insulin-like growth factorsmay be spinal cord, thyroid gland, used to treat patients with growth hormone receptor ovary, prostate, renal gland, deficiency (GHRD) (Fielder PJ, Gargosky SE, Vaccarello M, small intestine, heart, trachea, Wilson K, Cohen P, Diamond F, Guevara-Aguirre J, thymus, lymph node, and Rosenbloom AL, and Rosenfeld RG 1993. Acta Paediatr muscular system Suppl 388: 40-3). sbg34575SLITa An embodiment of the invention is the use of Cancer, infection, autoimmune sbg34575SLITa, a member of human slit-like proteins, which disorder, hematopoietic disorder, may be necessary for CNS development, and therefore can be wound healing disorder, useful for diagnosis and treatment of nervous and muscular inflammation, gastrointestinal diseases. A close homolog of sbg34575SLITa is leucine-rich ulceration, and diseases in repeat proteins(BAA85972, mouse ISLR), which also spinal cord, thyroid gland, demonstrates significant functions in neural development ovary, prostate, small intestine, (Nagasawa, A., Kudoh, J., Noda, S., Mashima, Y., Wright, A., heart, trachea, thymus, lymph Oguchi, Y., and Shimizu, N. Genomics 61 (1), 37-43, 1999). node, muscular system and It has been shown that expression of slit genes is associated with colon neuronal migration in the developing forebrain (Hu H, Neuron 23: 703-11, 1999). It is thus possible that similar molecules play a crucial role in the morphogenesis of the mammalian nervous system (Taniguchi H, Tohyama M, Takagi T. Brain Res Mol Brain Res 1996 36(1): 45-52). SBh71706.NIAP An embodiment of the invention is the use of Autoimmune disorder, SBh71706. NIAP in the suppression of apoptosis. Related hematopoietic disorder, wound polypeptides have been used for treating regulation of healing disorder, viral and cellular proliferation and differentiation and cell survival. bacterial infection, cancer, The NIAP prevent motor neuron apoptosis induced by a AIDS, amyotrophic lateral variey of signals. These proteins do contain 3 BIR( sclerosis, infertility, human Baculoviral Inhibitionof apoptosis protein repeats spinal muscular atrophy and (LISTON, P. Nature 379 (6563), 349-353 (1996). neurodegenerative disorder SBh77492.Breast An embodiment of the invention is the use of Cancer, autoimmune disorders, Specific BS200 SBh77492. Breast Specific BS200 in regulating vascular wound healing disorders, smooth muscle cell proliferation. A close homolog of infections, and hemotopoietic SBh77492. Breast Specific BS200 is EEGF protein. EEGF disorders protein is useful for enhancing neurological functions or treating neoplasia and other disorders (LI HS and OLSEN H, New isolated extracellular/epidermal growth factor, Patent Accession Number W79739, HUMAN GENOME SCI INC). sbg115305LRRa An embodiment of the invention is the use of Cancer, infection, autoimmune sbg115305LRRa, a disorder, hematopoietic disorder, Leucine-rich repeat (LRR) protein, in neuronal development wound healing disorder, and the adult nervous systems as cell adhesion molecules. inflammation, gastrointestinal Close homologs of sbg115305LRRa are connectin, slit, ulceration, diseases in spinal chaoptin, and toll. These LRR proteins possibly have cord, thyroid gland, heart, important roles in neuronal development and the adult trachea, thymus, lymph node, nervous systems as cell adhesion molecules (Taguchi A, muscular system, and nervous Wanaka A, Mori T, Matsumoto K, Imai Y, Tagaki T, system Tohyama M, 1996, Brain Res Mol Brain Res 35: 31-4). Leucine-rich repeat protein family has been implicated in protein-protein interactions, such as cell adhesion or receptor-ligand binding. At least one LRR was shown to be specifically expressed on B cells, suggesting its role in immunization (Miyake K, Yamashita Y, Ogata M, Sudo T, Kimoto M, 1995. J Immunol 154: 3333-40). Some studies have shown that brain injury can cause over expression of neuronal LRR, suggesting that neuronal LRR may be an important component of the pathophysiological response to brain injury (Ishii N, Wanaka A, Tohyama M, Brain Res Mol Brain Res 1996 Aug; 40(1): 148-52).

[0118] TABLE IV Quantitative, Tissue-specific mRNA expression detected using SybrMan Quantitative, tissue-specific, mRNA expression patterns of the genes were measured using SYBR-Green Quantitative PCR (Applied Biosystems, Foster City, CA; see Schmittgen T.D. et al., Analytical Biochemistry 285: 194-204, 2000) and human cDNAs prepared from various human tissues. Gene-specific PCR primers were designed using the first nucleic acid sequence listed in the Sequence List for each gene. Results are presented as the number of copies of each specific gene's mRNA detected in 1 ng mRNA pool from each tissue. Two replicate mRNA measurements were made from each tissue RNA. Tissue-Specific mRNA Expression (copies per ng mRNA; avg. ± range for 2 data points per tissue) Skeletal Spleen/ Gene Name Brain Heart Lung Liver Kidney muscle Intestine lymph Placenta Testis sbg10145 3389 ±  174 ±  187 ± 29  −6 ± 2  112 ± 4  64 ± 5  159 ± 7  147 ± 8  209 ± 37  563 ± 37 2SLITa  33  11 sbg29046  338 ±  385 ±  735 ± 29  138 ± 41  592 ± 36  218 ± 25  186 ± 35  348 ± 52  839 ± 65 46124 ± 22605 CYSa  60  69 sbg29046  951 ± 1121 ±  358 ± 110  364 ± 44  871 ± 128 1133 ± 203  347 ± 101  612 ± 18  601 ± 12  591 ± 51 CYSb  69  74 sbg37149 4989 ±  51 ±  457 ± 41  148 ± 12  769 ± 90  17 ± 2  31 ± 11  37 ± 14  10 ± 6  346 ± 10 SLITb  18  10 sbg36267 2976 ±  258 ±  127 ± 30   2 ± 0 1374 ± 13 2188 ± 72  44 ± 1  81 ± 5  113 ± 4  242 ± 1 SLIta  186  8 sbg35579 4630 ± 5518 ± 6114 ± 1422 1701 ± 140 5876 ± 1366 4017 ± 291 1918 ± 25 4310 ± 279 5247 ± 1  3589 ± 148 MELAa 1163 506 SBh69447.   1 ±   5 ±   6 ± 6  −7 ± 6   3 ± 0   1 ± 0  −2 ± 3   4 ± 1  200 ± 8   18 ± 7 Triglyceride   0  1 Lipase SBh86614.  742 ±  392 ±  487 ± 24  642 ± 6  576 ± 12  369 ± 53  234 ± 15  547 ± 25  662 ± 2  550 ± 4 Tryp 1  82  18 sbg106886 1308 ±  520 ±  340 ± 66  127 ± 11  418 ± 24  264 ± 39  130 ± 21  269 ± 21  538 ± 99  558 ± 116 DELTAa  49  19 sbg35779   2 ±   2 ±  21 ± 1  −4 ± 8   2 ± 1  −5 ± 8  26 ± 2  886 ± 38   7 ± 2   6 ± 5 THYa   1  1 sbg15130I   4 ±   6 ±  209 ± 2  −4 ± 6  42 ± 1  −2 ± 8   9 ± 5  14 ± 0  12 ± 4  133 ± 9 NHa   1  2 SBh26548.  56 ±  85 ±  111 ± 18  273 ± 1  149 ± 12  80 ± 17  86 ± 12  88 ± 8  120 ± 49   81 ± 35 home-box   3  5 sbg26991   1 ±   4 ±   2 ± 2   1 ± 3   4 ± 0  −1 ± 0   4 ± 0   2 ± 2   9 ± 0   26 ± 8 CERUa   0  2 sbg35851  83 ±  31 ±  37 ± 17  29 ± 5  53 ± 14  35 ± 8  17 ± 4  25 ± 13  36 ± 9   38 ± 3 PEROa  20  1 sbg36274 8770 ±  598 ±  591 ± 57   7 ± 5  518 ± 82  75 ± 9  253 ± 13 2847 ± 37  13 ± 1  278 ± 6 SLITa  345  8 sbg34575 2045 ±   2 ±   5 ± 0  −14 ± 2  −2 ± 4  −4 ± 3   0 ± 0  26 ± 7  10 ± 0   45 ± 6 SLITa  346  0 SBh71706.  251 ±  535 ± 1055 ± 55  122 ± 36  144 ± 7  322 ± 15  149 ± 5 1081 ± 67  740 ± 27  387 ± 17 NIAP   9  25 SBh77492.  154 ±  134 ± 1954 ± 135  325 ± 57  981 ± 13  60 ± 6  700 ± 15 1246 ± 5  586 ± 30  2614 ± 69 Breast   4  4 Specific BS200 sbg11965  43 ±  132 ±  25 ± 8  10 ± 7  122 ± 15  24 ± 10  22 ± 11  30 ± 8  15 ± 15  615 ± 4 2TYRa  11  21 sbg11530 7057 ±  289 ± 1122 ± 88  111 ± 4  547 ± 5 6178 ± 84  361 ± 12  896 ± 8  377 ± 18  9121 ± 120 5LRRa  326  1

[0119] TABLE V Additional diseases based on mRNA expression in specific tissues Tissue Expression Additional Diseases Brain Neurological and psychiatric diseases, including Alzheimers, parasupranuclear palsey, Huntington's disease, myotonic dystrophy, anorexia, depression, schizophrenia, headache, amnesias, anxiety disorders, sleep disorders, multiple sclerosis Heart Cardiovascular diseases, including congestive heart failure, dilated cardiomyopathy, cardiac arrhythmias, Hodgson's Disease, myocardial infarction, cardiac arrhythmias Lung Respiratory diseases, including asthma, Chronic Obstructive Pulmonary Disease, cystic fibrosis, acute bronchitis, adult respiratory distress syndrome Liver Dyslipidemia, hypercholesterolemia, hypertriglyceridemia, cirrhosis, hepatic encephalopathy, fatty hepatocirrhosis, viral and nonviral hepatitis, Type II Diabetes Mellitis, impaired glucose tolerance Kidney Renal diseases, including acute and chronic renal failure, acute tubular necrosis, cystinuria, Fanconi's Syndrome, glomerulonephritis, renal cell carcinoma, renovascular hypertension Skeletal muscle Eulenburg's Disease, hypoglycemia, obesity, tendinitis, periodic paralyses, malignant hyperthermia, paramyotonia congenita, myotonia congenita Intestine Gastrointestinal diseases, including Myotonia congenita, Ileus, Intestinal Obstruction, Tropical Sprue, Pseudomembranous Enterocolitis Spleen/lymph Lymphangiectasia, hypersplenism, angiomas, ankylosing spondylitis, Hodgkin's Disease, macroglobulinemia, malignant lymphomas, rheumatoid arthritis Placenta Choriocarcinoma, hydatidiform mole, placenta previa Testis Testicular cancer, male reproductive diseases, including low testosterone and male infertility Pancreas Diabetic ketoacidosis, Type 1 & 2 diabetes, obesity, impaired glucose tolerance

[0120]

1 52 1 2301 DNA Homo sapiens 1 atggaaaaag ttctttttta tctgtttctc attggcatag cagtgaaagc tcagatctgt 60 ccaaagcgtt gtgtctgtca gattttgtct cctaatcttg caaccctttg tgccaagaaa 120 gggcttttat ttgttccacc aaacattgac agaagaactg tggaactgcg gttggcagac 180 aattttgtta caaatattaa aaggaaagat tttgccaata tgaccagctt ggtggacctg 240 actctatcca ggaatacaat aagttttatt acacctcatg ctttcgctga cctacgaaat 300 ttgagggctt tgcatttgaa tagcaacaga ttgactaaaa ttacaaatga tatgttcagt 360 ggtctttcca atcttcatca tttgatactg aacaacaatc agctgacttt aatttcctct 420 acagcgtttg atgatgtctt cgcccttgag gagctggatc tgtcctataa taatctagaa 480 accattcctt gggatgctgt tgagaagatg gttagcttgc atacccttag tttggatcac 540 aatatgattg ataacattcc taaggggacc ttctcccatt tgcacaagat gactcggtta 600 gatgtgacat caaataaatt gcagaagcta ccacctgacc ctctctttca gcgagctcag 660 gtactagcaa cctcaggaat cataagccca tctacttttg cattaagttt tggtggaaac 720 cccttgcatt gcaattgtga attgttgtgg ttgaggcgtc tgtccagaga agatgactta 780 gagacctgtg cttctcctcc acttttaact ggccgctact tttggtcaat tcctgaagaa 840 gagtttttgt gtgagcctcc tctcattact cgtcatacac atgagatgag agtcctggag 900 ggacaaaggg caacactgag gtgcaaagcc aggggagacc ctgagcctgc aattcactgg 960 atttctcctg aagggaagct tatttcaaat gcaacaagat ctctggtgta tgataacgga 1020 acacttgaca ttcttatcac aactgtaaag gatacaggtg cttttacctg cattgcttcc 1080 aatcctgctg gggaagcaac acaaatagtg gatcttcata taattaagct ccctcactta 1140 ctaaatagta caaaccatat ccatgagcct gatcctggtt cttcagatat ctcaacttct 1200 accaagtcag gttctaatac aagcagtagt aatggtgata ctaaattgag tcaagataaa 1260 attgtggtgg cagaagctac atcatcaacg gcactactta aatttaattt tcaaagaaat 1320 atccctggaa tacgtatgtt tcaaatccag tacaatggta cttatgatga cacccttgtt 1380 tacagaatga tacctcctac gagcaaaact tttctggtca ataatctggc tgctggaact 1440 atgtatgact tgtgtgtctt ggccatatat gatgatggca tcacttccct cactgccaca 1500 agagtcgtgg gttgcatcca gtttactacg gaacaggatt atgtgcgttg ccatttcatg 1560 cagtctcagt ttttgggagg caccatgatt attattattg gtggaatcat tgtagcatct 1620 gtgctggtat tcatcattat tctgatgatc cggtataagg tttgcaacaa taatgggcaa 1680 cacaaggtca ccaaggttag caatgtttat tcccaaacta acggggctca aatacaaggc 1740 tgtagtgtaa cgctgcccca gtccgtgtcc aaacaagctg tgggacacga agagaatgcc 1800 cagtgttgta aagctaccag tgacaatgtg attcaatctt cagaaacttg ttcgagtcag 1860 gactcctcta ccactacctc tgctttgcct ccttcctgga cttcaagcac ttctgtgtcc 1920 caaaagcaga aaagaaagac tggcacaaag ccaagtacag aaccacagaa tgaagccgtc 1980 acaaatgttg aatcccaaaa cactaacagg aacaactcaa ctgccttgca gttagctagc 2040 cgtcctcccg attctgtcac agaggggccc acgtctaaaa gagcacatat aaagccaagt 2100 aagtttatca ctttgcctgc tgagagatcc ggagcaaggc acaagtactc cctcaatgga 2160 gaattaaagg aatactattg ttatattaac tcgccgaaca catgtggact gtttcctaaa 2220 agaagcatgt ctatgaatgt gatgtttatt cagtctgact gttctgatgg tcatagtgga 2280 aaggcaactc tcaaattctg a 2301 2 445 DNA Homo sapiens 2 aatgctgggc ctgccgtgga agggaggtct gtcctgggcg ctgctgctgc ttctcttagg 60 ctcccagatc ctgctgatct atgcctggca tttccacgag caaagggact gtgatgaaca 120 caatgtcatg gctcgttacc tccctgccac agtggagttt gctgtccaca cattcaacca 180 acagagcaag gactactatg cctacagact ggggcacatc ttgaattcct ggaaggagca 240 ggtggagtcc aagactgtat tctcaatgga gctactgctg gggagaacta ggtgtgggaa 300 atttgaagac gacattgaca actgccattt ccaagaaagc acagagctga acaatacttt 360 cacctgcttc ttcaccatca gcaccaggcc ctggatgact cagttcagcc tcctgaacaa 420 gacctgcttg gagggattcc actga 445 3 477 DNA Homo sapiens 3 atgtggagtc tgccgccgag cagggctctg tcctgtgcgc cactgctgct tctcttcagc 60 ttccagttcc tggttaccta tgcttggcgt ttccaagagg aagaggagtg gaatgaccaa 120 aaacaaattg ctgtttatct ccctcccacc ctggagtttg ccgtgtacac attcaacaag 180 cagagcaagg actggtatgc ctacaagctg gtgcctgtcc tggcttcctg gaaggagcag 240 ggttatgata agatgacatt ctccatgaat ctgcaactgg gcagaaccat gtgtgggaaa 300 tttgaagatg acattgacaa ctgccctttt caagagagcc cagagctgaa caatgtaaga 360 caagacacca gcttccctcc tggatacagc tgtggatgcc gcatggggtg tggtgcggac 420 acagacctgc acctgcttct tcaccattgg aatagagccc tggaggacac ggtttga 477 4 444 DNA Homo sapiens 4 atgtggagtc tgccgccgag cagggctctg tcctgtgcgc cactgctgct tctcttcagc 60 ttccagttcc tggttaccta tgcttggcgt ttccaagagg aagaggagtg gaatgaccaa 120 aaacaaattg ctgtttatct ccctcccacc ctggagtttg ccgtgtacac attcaacaag 180 cagagcaagg actggtatgc ctacaagctg gtgcctgtcc tggcttcctg gaaggagcag 240 ggttatgata agatgacatt ctccatgaat ctgcaactgg gcagaaccat gtgtgggaaa 300 tttgaagatg acattgacaa ctgccctttt caagagagcc cagagctgaa caatacctgc 360 acctgcttct tcaccattgg aatagagccc tggaggacac ggtttgacct ctggaacaag 420 acgtgctcag gcgggcattc ctga 444 5 2463 DNA Homo sapiens 5 atgctgcgcc tggggctgtg cgcggcggcg ctgctgtgcg tgtgccggcc gggtgccgtg 60 cgtgccgact gctggctcat tgagggcgac aagggctacg tgtggctggc catctgcagc 120 cagaaccagc cgccctacga gaccatcccg cagcacatca atagcaccgt gcacgacctg 180 cggctcaacg agaacaagct caaagccgtg ctctactcct cgctcaaccg ctttgggaac 240 ctcaccgacc tcaacctcac caagaacgag atctcctaca tcgaggacgg tgccttcctg 300 ggccagtcga gcctgcaggt cctgcagctg ggctacaaca agctcagcaa cctgacggag 360 ggcatgctgc gaggcatgag ccgcctgcag ttcctctttg tccagcacaa cctcatcgag 420 gtggtgacgc ccaccgcctt ctccgagtgc ccgagcctca tcagcatcga cctgtcctcc 480 aaccgcctca gccgcctgga cggtgccacc tttgccagcc tcgccagcct gatggtgtgt 540 gagctggccg gcaacccctt caactgtgag tgcgacctct tcggcttcct ggcctggctg 600 gtggtcttca acaacgtcac caagaactac gaccgcctgc agtgtgagtc gccgcgggag 660 tttgccggct acccgctgct ggtgccccgg ccctaccaca gcctcaacgc catcaccgta 720 ctccaggcca agtgtcggaa tggctcgctg cccgcccggc ccgtgagcca ccccacgccc 780 tactccaccg acgcccagag ggagccagac gagaactcgg gcttcaaccc cgacgagatc 840 ctttcggtgg agccgccggc ctcgtccacc acggatgcgt cggcagggcc agccatcaag 900 ctgcaccacg tcacgttcac ctcggccacc ctggtggtca tcatcccaca cccctacagc 960 aagatgtaca tcctcgtgca gtacaacaac agctacttct ccgacgtcat gaccctcaag 1020 aacaagaagg agatcgtgac gctggacaaa ctgcgggcgc acactgagta caccttctgc 1080 gtgacctcgc tgcgcaacag ccgccgcttc aaccacacct gcctgacctt caccacgcgg 1140 gaccccgtcc ccggagactt ggcgcccagc acctccacca ccacccacta catcatgacc 1200 atcctgggct gcctctttgg catggttatc gtgctgggag ccgtgtacta ctgcctgcgc 1260 aagcggcgca tgcaggagga gaagcagaag tctgtcaacg tcaagaagac catcctggag 1320 atgcgctacg gggctgatgt ggatgccggc tccattgtgc acgccgccca gaagctgggc 1380 gagcctcccg tgctgcccgt atctcgcatg gcctccatcc cctccatgat cggggagaag 1440 ctgcccaccg ccaaggggtt ggaggccggg ctggacacac ccaaggtagc caccaaaggc 1500 aactatatcg aggtgcgcac aggcgccggc ggggacggtc tggctcggcc cgaggatgac 1560 ctcccggacc tcgagaacgg ccagggctcg gctgcagaga tctccaccat tgccaaggag 1620 gtggacaagg tcaaccagat cattaacaac tgcatcgatg ctctcaagct ggactcggcc 1680 tcttttctgg gaggcggcag cagcagtggg gaccccgagc tggccttcga gtgccagtcc 1740 ctccctgcag ctgctgccgc ctcctcagcc actggccccg gggccctgga gcggcccagc 1800 ttcctttcgc ctccctacaa ggagagctcc caccacccac tacagcgcca gctgagcgcc 1860 gacgcggccg tgacccgcaa gacctgcagc gtgtcgtcca gtggttccat caagagcgcc 1920 aaggtcttta gcctggacgt gcccgaccat ccggccgcca cagggctggc taagggcgac 1980 tccaagtaca tcgagaaggg cagccccctc aacagcccgc tggaccggct cccgctggtg 2040 ccggcgggca gcggcggggg cagcggcggg ggcgggggca tccaccacct ggaggtgaag 2100 ccggcctacc actgcagcga gcaccggcac agctttcccg ccctgtacta cgaggagggt 2160 gccgacagcc tgagccagcg cgtgtccttc ctcaagccgc tgacccgctc caagcgtgac 2220 tccacctact cgcagctctc ccccagacac tactactcag ggtactcctc cagccccgag 2280 tactcatccg agagcacgca caagatctgg gagcgcttcc ggccctacaa gaagcaccac 2340 cgggaggagg tgtacatggc cgccggtcac gccctgcgca agaaggtcca gttcgccaag 2400 gacgaggatc tgcatgacat ccttgattac tggaaggggg tctccgccca gcagaagctg 2460 tga 2463 6 2601 DNA Homo sapiens 6 atgaccattg aaaaaatgtt ttctttttat tttttagatt atttctcttt attcagaagc 60 atacagttgt ttgctgattg caagaagatg tttctgtggc tgtttctgat tttgtcagcc 120 ctgatttctt cgacaaatgc agattctgac atatcggtgg aaatttgcaa tgtgtgttcc 180 tgcgtgtcag ttgagaatgt gctctatgtc aactgtgaga aggtttcagt ctacagacca 240 aatcagctga aaccaccttg gtctaatttt tatcacctca atttccaaaa taatttttta 300 aatattctgt atccaaatac attcttgaat ttttcacatg cagtctccct gcatctgggg 360 aataataaac tgcagaacat tgagggagga gcctttcttg ggctcagtgc attaaagcag 420 ttgcacttga acaacaatga attaaagatt ctccgagctg acactttcct tggcatagag 480 aacttggagt atctccaggc tgactacaat ttaatcaagt atattgaacg aggagccttc 540 aataagctcc acaaactgaa agttctcatt cttaatgaca atctgatttc attccttcct 600 gataatattt tccgattcgc atctttgacc catctggata tacgagggaa cagaatccag 660 aagctccctt atatcggggt tctggaacac attggccgtg tcgttgaatt gcaactggaa 720 gataaccctt ggaactgtag ctgtgattta ttgcccttaa aagcttggct ggagaacatg 780 ccatataaca tttacatagg agaagctatc tgtgaaactc ccagtgactt atatggaagg 840 cttttaaaag aaaccaacaa acaagagcta tgtcccatgg gcaccggcag tgattttgac 900 gtgcgcatcc tgcctccatc tcagctggaa aatggctaca ccactcccaa tggtcacact 960 acccaaacat ctttacacag attagtaact aaaccaccaa aaacaacaaa tccttccaag 1020 atctctggaa tcgttgcagg caaagccctc tccaaccgca atctcagtca gattgtgtct 1080 taccaaacaa gggtgcctcc tctaacacct tgcccggcac cttgcttctg caaaacacac 1140 ccttcagatt tgggactaag tgtgaactgc caagagaaaa atatacagtc tatgtctgaa 1200 ctgataccga aacctttaaa tgcgaagaag ctgcacgtca atggcaatag catcaaggat 1260 gtggacgtat cagacttcac tgactttgaa ggactggatt tgcttcattt aggcagcaat 1320 caaattacag tgattaaggg agacgtattt cacaatctca ctaatttacg caggctatat 1380 ctcaatggca atcaaattga gagactctat cctgaaatat tttcaggtct tcataacctg 1440 cagtatctgt atttggaata caatttgatt aaggaaatct cagcaggcac ctttgactcc 1500 atgccaaatt tgcagttact gtacttaaac aataatctcc taaagagcct gcctgtttac 1560 atcttttccg gagcaccctt agctagactg aacctgagga acaacaaatt catgtacctg 1620 cctgtcagtg gggtccttga tcagttgcaa tctcttacac agattgactt ggagggcaac 1680 ccatgggact gtacttgtga cttggtggca ttaaagctgt gggtggagaa gttgagcgac 1740 gggattgttg tgaaagaact gaaatgtgag acgcctgttc agtttgccaa cattgaactg 1800 aagtccctca aaaatgaaat cttatgtccc aaacttttaa ataagccgtc tgcaccattc 1860 acaagccctg cacctgccat tacattcacc actcctttgg gtcccattcg aagtcctcct 1920 ggtgggccag tgcctctgtc tattttaatc ttaagtatct tagtggtcct cattttaacg 1980 gtgtttgttg ctttttgcct tcttgttttt gtcctgcgac gcaacaagaa acccacagtg 2040 aagcacgaag gcctggggaa tcctgactgt ggctccatgc agctgcagct aaggaagcat 2100 gaccacaaaa ccaataaaaa agatggactg agcacagaag ctttcattcc acaaactata 2160 gaacagatga gcaagagcca cacttgtggc ttgaaagagt cagaaactgg gttcatgttt 2220 tcagatcctc caggacagaa agttgttatg agaaatgtgg ccgacaagga gaaagattta 2280 ttacatgtag ataccaggaa gagactgagc acaattgatg agctggatga attattccct 2340 agcagggatt ccaatgtgtt tattcagaat tttcttgaaa gcaaaaagga gtataatagc 2400 ataggtgtca gtggctttga gatccgctat ccagaaaaac aaccagacaa aaaaagtaag 2460 aagtcactga taggtggcaa ccacagtaaa attgttgtgg aacaaaggaa gagtgagtat 2520 tttgaactga aggcgaaact gcagagttcc cctgactacc tacaggtcct tgaggagcaa 2580 acagctttga acaagatcta g 2601 7 1602 DNA Homo sapiens 7 atggctccag gacccttctc ctcggccctc ctctcgccgc cgcccgctgc cctgcccttt 60 ctgctgctgc tctgggcggg ggcatctcgt ggccagccct gccccggccg ctgcatctgc 120 cagaacgtgg cgcccacact gacaatgctg tgcgccaaga ccggcttgct ctttgtgccg 180 cccgccatcg accggcgcgt ggtggagctg cggctcaccg acaacttcat cgccgccgtg 240 cgccgccgag acttcgccaa catgaccagc ctggtgcacc tcactctctc ccggaacacc 300 atcggccagg tggcagctgg cgccttcgcc gacctgcgtg ccctccgggc cctgcacctg 360 gacagcaacc gcctggcgga ggtgcgcggc gaccagctcc gcggcctggg caacctccgc 420 cacctgatcc ttggaaacaa ccagatccgc cgggtggagt cggcggcctt tgacgccttc 480 ctgtccaccg tggaggacct ggatctgtcc tacaacaacc tggaggccct gccgtgggag 540 gcggtgggcc agatggtgaa cctaaacacc ctcacgctgg accacaacct catcgaccac 600 atcgcggagg ggaccttcgt gcagcttcac aagctggtcc gtctggacat gacctccaac 660 cgcctgcata aactcccgcc cgacgggctc ttcctgaggt cgcagggcac cgggcccaag 720 ccgcccaccc cgctgaccgt cagcttcggc ggcaaccccc tgcactgcaa ctgcgagctg 780 ctctggctgc ggcggctgac ccgcgaggac gacttagaga cctgcgccac gcccgaacac 840 ctcaccgacc gctacttctg gtccatcccc gaggaggagt tcctgtgtga gcccccgctg 900 atcacacggc aggcgggggg ccgggccctg gtggtggaag gccaggcggt gagcctgcgc 960 tgccgagcgg tgggtgaccc cgagccggtg gtgcactggg tggcacctga tgggcggctg 1020 ctggggaact ccagccggac ccgggtccgg ggggacggga cgctggatgt gaccatcacc 1080 accttgaggg acagtggcac cttcacttgt atcgcctcca atgctgctgg ggaagcgacg 1140 gcgcccgtgg aggtgtgcgt ggtacctctg cctctgatgg cacccccgcc ggctgccccg 1200 ccgcctctca ccgagcccgg ctcctctgac atcgccacgc cgggcagacc aggtgccaac 1260 gattctgcgg ctgagcgtcg gctcgtggca gccgagctca cctcgaactc cgtgctcatc 1320 cgctggccag cccagaggcc tgtgcccgga atacgcatgt accaggttca gtacaacagt 1380 tccgttgatg actccctcgt ctacagctct gcctccctca tgcacattgt agagcaccag 1440 ttaaatgctt cagtcatctg cttggcttca cctggagatg ccagcggggc tggagctgtt 1500 tccctacctg tggagagcct cagctcctgg ctgtcagatc ttcaccgaga aacctgcctc 1560 ttggcctcca tctctgcctt tccagtgttt tcttggccat ag 1602 8 2316 DNA Homo sapiens 8 atggctccag gacccttctc ctcggccctc ctctcgccgc cgcccgctgc cctgcccttt 60 ctgctgctgc tctgggcggg ggcatctcgt ggccagccct gccccggccg ctgcatctgc 120 cagaacgtgg cgcccacact gacaatgctg tgcgccaaga ccggcttgct ctttgtgccg 180 cccgccatcg accggcgcgt ggtggagctg cggctcaccg acaacttcat cgccgccgtg 240 cgccgccgag acttcgccaa catgaccagc ctggtgcacc tcactctctc ccggaacacc 300 atcggccagg tggcagctgg cgccttcgcc gacctgcgtg ccctccgggc cctgcacctg 360 gacagcaacc gcctggcgga ggtgcgcggc gaccagctcc gcggcctggg caacctccgc 420 cacctgatcc ttggaaacaa ccagatccgc cgggtggagt cggcggcctt tgacgccttc 480 ctgtccaccg tggaggacct ggatctgtcc tacaacaacc tggaggccct gccgtgggag 540 gcggtgggcc agatggtgaa cctaaacacc ctcacgctgg accacaacct catcgaccac 600 atcgcggagg ggaccttcgt gcagcttcac aagctggtcc gtctggacat gacctccaac 660 cgcctgcata aactcccgcc cgacgggctc ttcctgaggt cgcagggcac cgggcccaag 720 ccgcccaccc cgctgaccgt cagcttcggc ggcaaccccc tgcactgcaa ctgcgagctg 780 ctctggctgc ggcggctgac ccgcgaggac gacttagaga cctgcgccac gcccgaacac 840 ctcaccgacc gctacttctg gtccatcccc gaggaggagt tcctgtgtga gcccccgctg 900 atcacacggc aggcgggggg ccgggccctg gtggtggaag gccaggcggt gagcctgcgc 960 tgccgagcgg tgggtgaccc cgagccggtg gtgcactggg tggcacctga tgggcggctg 1020 ctggggaact ccagccggac ccgggtccgg ggggacggga cgctggatgt gaccatcacc 1080 accttgaggg acagtggcac cttcacttgt atcgcctcca atgctgctgg ggaagcgacg 1140 gcgcccgtgg aggtgtgcgt ggtacctctg cctctgatgg cacccccgcc ggctgccccg 1200 ccgcctctca ccgagcccgg ctcctctgac atcgccacgc cgggcagacc aggtgccaac 1260 gattctgcgg ctgagcgtcg gctcgtggca gccgagctca cctcgaactc cgtgctcatc 1320 cgctggccag cccagaggcc tgtgcccgga atacgcatgt accaggttca gtacaacagt 1380 tccgttgatg actccctcgt ctacaggatg atcccgtcca ccagtcagac cttcctggtg 1440 aatgacctgg cggcgggccg tgcctacgac ttgtgcgtgc tggcggtcta cgacgacggg 1500 gccacagcgc tgccggcaac gcgagtggtg ggctgtgtac agttcaccac cgctggggat 1560 ccggcgccct gccgcccgct gagggcccat ttcttgggcg gcaccatgat catcgccatc 1620 gggggcgtca tcgtcgcctc ggtcctcgtc ttcatcgttc tgctcatgat ccgctataag 1680 gtgtatggcg acggggacag ccgccgcgtc aagggctcca ggtcgctccc gcgggtcagc 1740 cacgtgtgct cgcagaccaa cggcgcaggc acaggcgcgg cacaggcccc ggccctgccg 1800 gcccaggacc actacgaggc gctgcgcgag gtggagtccc aggctgcccc cgccgtcgcc 1860 gtcgaggcca aggccatgga ggccgagacg gcatccgcgg agccggaggt ggtccttgga 1920 cgttctctgg gcggctcggc cacctcgctg tgcctgctgc catccgagga aacttccggg 1980 gaggagtctc gggccgcggt gggccctcga aggagccgat ccggcgccct ggagccacca 2040 acctcggcgc cccctactct agctctagtt cctgggggag ccgcggcccg gccgaggccg 2100 cagcagcgct attcgttcga cggggactac ggggcactat tccagagcca cagttacccg 2160 cgccgcgccc ggcggacaaa gcgccaccgg tccacgccgc acctggacgg ggctggaggg 2220 ggcgcggccg gggaggatgg agacctgggg ctgggctccg ccagggcgtg cctggctttc 2280 accagcaccg agtggatgct ggagagtacc gtgtga 2316 9 1200 DNA Homo sapiens 9 atgtggcagc ttttagcagc agcatgctgg atgcttcttc ttggatctat gtatggttat 60 gacaagaaag gaaacaatgc aaaccctgaa gctaatatga atattagcca gattatttct 120 tactggggtt atccttatga agagtatgat gttacaacaa aagatggtta tatccttgga 180 atttatagga ttccacatgg aagaggatgc ccagggagga cagctccaaa gcctgctgtg 240 tatttgcagc atggcttaat tgcatctgcc agtaactgga tttgcaacct gcccaacaac 300 agtttggctt tccttctggc agatagtggt tatgacgtgt ggttggggaa cagccgagga 360 aacacttggt ccagaaaaca ccttaaattg tcaccgaaat caccagaata ctgggccttc 420 agtttggatg agatggctaa atatgacctt ccagccacaa tcaattttat catagagaaa 480 actggacaga agcgactcta ctacgtgggc cactcacaag gcaccaccat agcttttata 540 gcattttcta caaacccaga actggctaaa aagattaaga tattttttgc actggctcca 600 gttgtcacag ttaaatacac ccaaagtcct atgaaaaaac taacaaccct ttccaggcga 660 gtagttaagg tgttgtttgg tgacaaaatg ttccaccctc atacattgtt tgaccaattc 720 attgccacca aagtgtgcaa tcgaaagcta ttccgtcgta tttgcagcaa cttcctattt 780 actctgagtg gatttgatcc gcaaaactta aatatgagtc gcttggatgt ttatttgtca 840 cacaatcctg cgggaacatc tgttcagaat atgctgcact gggctcaggc tgttaattct 900 ggtcagctcc aagcttttga ttggggaaac tctgatcaga acatgatgca cttccaccag 960 cttacacctc ctttatacaa cattactaag atcgaagttc caacagcaat atggaatggt 1020 ggacaggaca ttgtggctga tcccaaggat gttgaaaatt tacttcctca aattgctaac 1080 cttatttatt acaagctgat tccacactac aatcatgtgg atttttacct tggagaggat 1140 gcacctcagg aaatttacca agacctaatt atattgatgg aagaatattt acaaaattaa 1200 10 768 DNA Homo sapiens 10 atcgtggggg gctcaaacgc gcagccgggc acctggcctt ggcaagtgag cctgcaccat 60 ggaggtggcc acatctgcgg gggctccctc atcgccccct cctgggtcct ctccgctgct 120 cactgtttca tgacggggcg gcagtaccgc tgcccggaga cccgccgcac gcgctctgcc 180 ctgcctacca ggaaaaggag gagggcctat aaccactaca gccagggctc agacctggcc 240 ctgctgcagc tcgcccaccc cacgacccac acacccctct gcctgcccca gcccgcccat 300 cgcttcccct ttggagcctc ctgctgggcc actggctggg atcaggacac cagtgatgcc 360 ccgtctcttt caccagctcc tgggacccta cgcaatctgc gcctgcgtct catcagtcgc 420 cccacatgta actgtatcta caaccagctg caccagcgac acctgtccaa cccggcccgg 480 cctgggatgc tatgtggggg cccccagcct ggggtgcagg gcccctgtca gggcttgttt 540 ggggcaccac tggtgcatga ggtgaggggc acatggttcc tggccgggct gcacagtttc 600 ggagatgctt gccaaggccc cgccaggccg gcggtcttca ccgcgctccc tgctatgagg 660 actgggtcag cagtttggac tcggcaggtc tacttcgccg aggaaccaga gcccgaggct 720 gagcctggaa gctgcctggc caacataaga cccttctctc tccagtga 768 11 906 DNA Homo sapiens 11 atggagactg ctgggagtga ttgggttgca ggaggcccac tgacccaggc ctctcacccc 60 tcagagtgcg ggaaggcccc gcggccaggg gcctggccct gggaggccca ggtgatggtg 120 ccaggatcca gaccctgcca tggggcgctg gtgtctgaaa gctgggtctt ggcacctgcc 180 agctgctttc tggagcaagt aacacacaca ctttgttgct gcagaatgac tcgcgttgga 240 gccttttgtg ccaggaggag gggacctggt ttctggctgg aatcagagac tttcccagtg 300 gctgtctact tgcccagggc ctataaccac tacagccagg gctcagacct ggccctgctg 360 cagctcgccc accccacgac ccacacaccc ctctgcctgc cccagcccgc ccatcgcttc 420 ccctttggag cctcctgctg ggccactggc tgggatcagg acaccagtga tgctcctggg 480 accctacgca atctgcgcct gcgtctcatc agtcgcccca catgtaactg tatctacaac 540 cagctgcacc agcgacacct gtccaacccg gcccggcctg ggatgctatg tgggggcccc 600 cagcctgggg tgcagggccc ctgtcagggc ttgtttgggg caccactggt gcatgaggtg 660 aggggcacat ggttcctggc cgggctgcac agtttcggag atgcttgcca aggccccgcc 720 aggccggcgg tcttcaccgc gctccctgct atgaggactg ggtcagcagt ttggactcgg 780 caggtctact tcgccgagga accagagccc gaggctgagc ctggaagctg cctggccaac 840 ataagtatgt ggccccgggg cctcctgcca aaccctgcct ctccaggacc cttctctctc 900 cagtga 906 12 1152 DNA Homo sapiens 12 atgcccagcg gctgccgctg cctgcatctc gtgtgcctgt tgtgcattct gggggctccc 60 ggtcagcctg tccgagccga tgactgcagc tcccactgtg acctggccca cggctgctgt 120 gcacctgacg gctcctgcag gtgtgacccg ggctgggagg ggctgcactg tgagcgctgt 180 gtgaggatgc ctggctgcca gcacggtacc tgccaccagc catggcagtg catctgccac 240 agtggctggg caggcaagtt ctgtgacaaa gatgaacata tctgtaccac gcagtccccc 300 tgccagaatg gaggccagtg catgtatgac gggggcggtg agtaccattg tgtgtgctta 360 ccaggcttcc atgggcgtga ctgcgagcgc aaggctggac cctgtgaaca ggcaggctcc 420 ccatgccgca atggcgggca gtgccaggac gaccagggct ttgctctcaa cttcacgtgc 480 cgctgcttgg tgggctttgt gggtgcccgc tgtgaggtaa atgtggatga ctgcctgatg 540 cggccttgtg ctaacggtgc cacctgcctt gacggcataa accgcttctc ctgcctctgt 600 cctgagggct ttgctggacg cttctgcacc atcaacctgg atgactgtgc cagccgccca 660 tgccagagag gggcccgctg tcgggaccgt gtccatgact tcgactgcct ctgccccagt 720 ggctatggtg gcaagacttg tgagcttgtc ttacctgtcc cagacccccc aaccacagtg 780 gacacccctc tagggcccac ctcagctgta gtggtacctg ccacggggcc agccccccac 840 agcgcagggg ctggtctgct gcggatctca gtgaaggagg tggtgcggag gcaagaggct 900 gggctaggtg agcctagctt ggtggccctg gtggtgtttg gggccctcac tgctgccctg 960 gttctggcta ctgtgttgct gaccctgagg gcctggcgcc ggggtgtctg cccccctgga 1020 ccctgttgct accctgcccc acactatgct ccagcgtgcc aggaccagga gtgtcaggtt 1080 agcatgctgc cagcagggct ccccctgcca cgtgacttgc cccctgagcc tggaaagacc 1140 acagcactgt ga 1152 13 1254 DNA Homo sapiens 13 atggcatctt acctttatgg agtactcttt gctgttggcc tctgtgctcc aatctactgt 60 gtgtccccgg ccaatgcccc cagtgcatac ccccgccctt cctccacaaa gagcacccct 120 gcctcacagg tgtattccct caacaccgac tttgccttcc gcctataccg caggctggtt 180 ttggagaccc cgagtcagaa catcttcttc tcccctgtga gtgtctccac ttccctggcc 240 atgctctccc ttggggccca ctcagtcacc aagacccaga ttctccaggg cctgggcttc 300 aacctcacac acacaccaga gtctgccatc caccagggct tccagcacct ggttcactca 360 ctgactgttc ccagcaaaga cctgaccttg aagatgggaa gtgccctctt cgtcaagaag 420 gagctgcagc tgcaggcaaa tttcttgggc aatgtcaaga ggctgtatga agcagaagtc 480 ttttctacag atttctccaa cccctccatt gcccaggcga ggatcaacag ccatgtgaaa 540 aagaagaccc aagggaaggt tgtagacata atccaaggcc ttgaccttct gacggccatg 600 gttctggtga accacatttt ctttaaagcc aagtgggaga agccctttca ccctgaatat 660 acaagaaaga acttcccatt cctggtgggc gagcaggtca ctgtgcatgt ccccatgatg 720 caccagaaag agcagttcgc ttttggggtg gatacagagc tgaactgctt tgtgctgcag 780 atggattaca agggagatgc cgtggccttc tttgtcctcc ctagcaaggg caagatgagg 840 caactggaac aggccttgtc agccagaaca ctgagaaagt ggagccactc actccagaaa 900 aggtggatag aggtgttcat ccccagattt tccatttctg cctcctacaa tctggaaacc 960 atcctcccga agatgggcat ccaaaatgtc tttgacaaaa atgctgattt ttctggaatt 1020 gcaaagagag actccctgca ggtttctaaa gcaacccaca aggctgtgct ggatgtcagt 1080 gaagagggca ctgaggccac agcagctacc accaccaagt tcatagtccg atcgaaggat 1140 ggcccctctt acttcactgt ctccttcaat aggaccttcc tgatgatgat tacaaataaa 1200 gccacagacg gtattctctt tctagggaaa gtggaaaatc ccactaaatc ctag 1254 14 732 DNA Homo sapiens 14 atggggtcca gcagcttctt ggtcctcatg gtgtctctcg ttcttgtgac cctggtggct 60 gtggaaggag ttaaagaggg tatagagaaa gcaggggttt gcccagctga caacgtacgc 120 tgcttcaagt ccgatcctcc ccagtgtcac acagaccagg actgtctggg ggaaaggaag 180 tgttgttacc tgcactgtgg cttcaagtgt gtgattcctg tgaaggaact ggaagaaggt 240 cagcgcttat tacataaccg tgagcttcct ccagctgcaa tattaggaga ttctcttaca 300 gagaaatcgg ggggctgccc gccagatgat gggccctgcc tcctatcggt gcctgaccag 360 tgcgtggaag acagccagtg tcccttgacc aggaagtgct gctacagagc ttgcttccgc 420 cagtgtgtcc ccagggtctc tggtaaatgc ctcccctcca ccttgctgac catccaagcc 480 ccaagcttca gggccagtgg gcaaggacgg agctcaccca gttccctgtg ttgcagtgaa 540 gctgggcagc tgcccagagg accaactgcg ctgcctcagc cccatgaacc acctgtgtca 600 caaggactca gactgctcgg gcaaaaagcg atgctgccac agcgcctgcg ggcgggattg 660 ccgggatcct gccagaggta cggctcctgg gtgcccaggg caggtgcctc ccctctccga 720 gcccagctct aa 732 15 558 DNA Homo sapiens 15 atggggtcca gcagcttctt ggtcctcatg gtgtctctcg ttcttgtgac cctggtggct 60 gtggaaggag ttaaagaggg tatagagaaa gcaggggttt gcccagctga caacgtacgc 120 tgcttcaagt ccgatcctcc ccagtgtcac acagaccagg actgtctggg ggaaaggaag 180 tgttgttacc tgcactgtgg cttcaagtgt gtgattcctg tgaaggaact ggaagaagtt 240 ccctgtgttg cagtgaagct gggcagctgc ccagaggacc aactgcgctg cctcagcccc 300 atgaaccacc tgtgtcacaa ggactcagac tgctcgggca aaaagcgatg ctgccacagc 360 gcctgcgggc gggattgccg ggatcctgcc agaggtacgg ctcctgggtg cccagggcag 420 gtgcctcccc tctccgagcc cagctctaat actttcttca ttgctacaag cttaacagga 480 tgcctcccca gaagtcagga cctcccatgg ccaggattag gaaactggat aggggttgga 540 ggagtcctgc taggatga 558 16 597 DNA Homo sapiens 16 atgaactcgg gacgcgagcc ccgaacaccc cggacactct taagcatcgc agacatccta 60 gccccgcgca tggtcccccg agcaccctct gcgccgcagc ttccagagtc gggtccgggt 120 ccaacgtcgc cgctgtgcgc gctggaggag ctgactagta aaactttccg cggacttgac 180 gcgcgcgctc tgcagccctc tgaagggcgg gcaggtccgg acgcgctggg ccctggtccc 240 ttcggccgca aacggcgcaa gtcacgcact gcgttcaccg cgcaacaggt gctggagctg 300 gagcggcgct tcgtcttcca gaagtacctg gcgccgtccg agcgagacgg gctagctacg 360 cgactcggcc tggccaacgc gcaggtggtc acttggttcc agaaccggcg agccaagctc 420 aagcgcgatg tggaggagat gcgcgccgac gtcgcctcgc tacgcgcgtt gtccccggaa 480 gtcctgtgca gcttagcact gcccgaaggc gctccagatc ccggcctctg cctcggccct 540 gccggccctg actcccggcc ccacctgtca gacgaggaga tacaggtgga cgattga 597 17 993 DNA Homo sapiens 17 atggtatgga aaagagagaa tttctacaag gaggtcaagc gaggaagagc tttgttttta 60 aaaaggcttt gtattttcaa tattgatact gataatacat ttcaaaggat cattgaaaaa 120 ccatcctggt tgggattttt aggtccaatg attaaagcag agactggaga cttcatttat 180 gtacatgtaa aaaataatgc ttcaagagct tatagttatc atcctcatgg gctcacctac 240 tccaaagaaa atgaaggtgc tatctatcct gataatacga caggcctgca aaaggaagat 300 gaatatctgg agccagggaa acaatatacc tacaagtggt atgtagaaga acatcaggga 360 cctggcccca atgacagtaa ttgtgtgaca agaatttacc attcccatat agacactgca 420 agagatgtag cttcgggact tattggacca atactgactt gtaaaagagc aataaatgga 480 tacatctatg gaaatctgcc caatctcacc atgtgtgctg aagatagggt ccagtggtat 540 tttgttggca tgggtggcgt ggctgacata caccccgtct acctccgcgg acaaactctg 600 atctctcgga atcacagaaa ggacaccatt atgctcttcc cctcctcact ggaagatgcc 660 ttcatggtgg ccaaggcccc tggagtgtgg atgctgggat gccagataca tggtagtgat 720 atattacttt tgcgtgatac aaagtcagag aacttccaag ggcttagccc attccacatg 780 catttcctta caaatgaaga gacctatatc caagaagaga gtatgcaggc atttttcaaa 840 gtaagtaatt gccagaaacc ttcaacagaa gcctttgtta ctgggacaca tgttatacat 900 tactatattg ctgctaaaga aattctttgg aactatgctc catctggtat agatttcttc 960 actaaaaaaa atttaacagc agctggaagg taa 993 18 1440 DNA Homo sapiens 18 atggccatcc tcccgttgct cctgtgcctg ctgccgctgg cccctgcctc atccccaccc 60 cagtcagcca cacccagccc atgtccccgc cgctgccgct gccagacaca gtcgctgccc 120 ctaagcgtgc tgtgcccagg ggcaggcctc ctgttcgtgc caccctcgct ggaccgccgg 180 gcagccgagc tgcggctggc agacaacttc atcgcctccg tgcgccgccg cgacctggcc 240 aacatgacag gcctgctgca tctgagcctg tcgcggaaca ccatccgcca cgtggctgcc 300 ggcgccttcg ccgacctgcg ggccctgcgt gccctgcacc tggatggcaa ccggctgacc 360 tcactgggcg agggccagct gcgcggcctg gtcaacttgc gccacctcat cctcagcaac 420 aaccagctgg cagcgctggc ggccggcgcc ctggatgatt gtgccgagac actggaggac 480 ctcgacctct cctacaacaa cctcgagcag ctgccctggg aggccctggg ccgcctgggc 540 aacgtcaaca cgttgggcct cgaccacaac ctgctggctt ctgtgcccgc cggcgctttt 600 tcccgcctgc acaagctggc ccggctggac atgacctcca accgcctgac cacaatccca 660 cccgacccac tcttctcccg cctgcccctg ctcgccaggc cccggggctc gcccgcctct 720 gccctggtgc tggcctttgg cgggaacccc ctgcactgca actgcgagct ggtgtggctg 780 cgtcgcctgg cgcgggagga cgacctcgag gcctgcgcgt ccccacctgc tctgggcggc 840 cgctacttct gggcggtggg cgaggaggag tttgtctgcg agccgcccgt ggtgactcac 900 cgctcaccac ctctggctgt gcccgcaggt cggccggctg ccctgcgctg ccgggcagtg 960 ggggacccag agccccgtgt gcgttgggtg tcaccccagg gccggctgct aggcaactca 1020 agccgtgccc gcgccttccc caatgggacg ctggagctgc tggtcaccga gccgggtgat 1080 ggtggcatct tcacctgcat tgcggccaat gcagctggcg aggccacagc tgctgtggag 1140 ctgactgtgg gtcccccacc acctcctcag ctagccaaca gcaccagctg tgaccccccg 1200 cgggacgggg atcctgatgc tctcacccca ccctccgctg cctctgcttc tgccaaggtg 1260 gccgacactg ggccccctac cgaccgtggc gtccaggtga ctgagcacgg ggccacagct 1320 gctcttgtcc agtggccgga tcagcggcct atcccgggca tccgcatgta ccagatccag 1380 tacaacagct cggctgatga catcctcgtc tacaggtgca gggtccaggc actggggtag 1440 19 1887 DNA Homo sapiens 19 atggccatcc tcccgttgct cctgtgcctg ctgccgctgg cccctgcctc atccccaccc 60 cagtcagcca cacccagccc atgtccccgc cgctgccgct gccagacaca gtcgctgccc 120 ctaagcgtgc tgtgcccagg ggcaggcctc ctgttcgtgc caccctcgct ggaccgccgg 180 gcagccgagc tgcggctggc agacaacttc atcgcctccg tgcgccgccg cgacctggcc 240 aacatgacag gcctgctgca tctgagcctg tcgcggaaca ccatccgcca cgtggctgcc 300 ggcgccttcg ccgacctgcg ggccctgcgt gccctgcacc tggatggcaa ccggctgacc 360 tcactgggcg agggccagct gcgcggcctg gtcaacttgc gccacctcat cctcagcaac 420 aaccagctgg cagcgctggc ggccggcgcc ctggatgatt gtgccgagac actggaggac 480 ctcgacctct cctacaacaa cctcgagcag ctgccctggg aggccctggg ccgcctgggc 540 aacgtcaaca cgttgggcct cgaccacaac ctgctggctt ctgtgcccgc cggcgctttt 600 tcccgcctgc acaagctggc ccggctggac atgacctcca accgcctgac cacaatccca 660 cccgacccac tcttctcccg cctgcccctg ctcgccaggc cccggggctc gcccgcctct 720 gccctggtgc tggcctttgg cgggaacccc ctgcactgca actgcgagct ggtgtggctg 780 cgtcgcctgg cgcgggagga cgacctcgag gcctgcgcgt ccccacctgc tctgggcggc 840 cgctacttct gggcggtggg cgaggaggag tttgtctgcg agccgcccgt ggtgactcac 900 cgctcaccac ctctggctgt gcccgcaggt cggccggctg ccctgcgctg ccgggcagtg 960 ggggacccag agccccgtgt gcgttgggtg tcaccccagg gccggctgct aggcaactca 1020 agccgtgccc gcgccttccc caatgggacg ctggagctgc tggtcaccga gccgggtgat 1080 ggtggcatct tcacctgcat tgcggccaat gcagctggcg aggccacagc tgctgtggag 1140 ctgactgtgg gtcccccacc acctcctcag ctagccaaca gcaccagctg tgaccccccg 1200 cgggacgggg atcctgatgc tctcacccca ccctccgctg cctctgcttc tgccaaggtg 1260 gccgacactg ggccccctac cgaccgtggc gtccaggtga ctgagcacgg ggccacagct 1320 gctcttgtcc agtggccgga tcagcggcct atcccgggca tccgcatgta ccagatccag 1380 tacaacagct cggctgatga catcctcgtc tacaggatga tcccggcgga gagccgctcg 1440 ttcctgctga cggacctggc gtcaggccgg acctacgatc tgtgcgtgct cgccgtgtat 1500 gaggacagcg ccacggggct cacggccacg cggcctgtgg gctgcgcccg cttctccacc 1560 gaacctgcgc tgcggccatg cggggcgccg cacgctccct tcctgggcgg cacgatgatc 1620 atcgcgctgg gcggcgtcat cgtagcctcg gtactggtct tcatcttcgt gctgctaatg 1680 cgctacaagg tgcacggcgg ccagcccccc ggcaaggcca agattcccgc gcctgttagc 1740 agcgtttgct cccagaccaa cggcgccctg ggccccacgc ccacgcccgc cccgcccgcc 1800 ccggagcccg cggcgctcag ggcccacacc gtggtccagc tggactgcga gccctggggg 1860 cccggccacg aacctgtggg accctag 1887 20 2538 DNA Homo sapiens 20 atgctgagcg gcgtttggtt cctcagtgtg ttaaccgtgg ccgggatctt acagacagag 60 agtcgcaaaa ctgccaaaga catttgcaag atccgctgtc tgtgcgaaga aaaggaaaac 120 gtactgaata tcaactgtga gaacaaagga tttacaacag ttagcctgct ccagcccccc 180 cagtatcgaa tctatcagct ttttctcaat ggaaacctct tgacaagact gtatccaaac 240 gaatttgtca attactccaa cgcggtgact cttcacctag gtaacaacgg gttacaggag 300 atccgaacgg gggcattcag tggcctgaaa actctcaaaa gactgcatct caacaacaac 360 aagcttgaga tattgaggga ggacaccttc ctaggcctgg agagcctgga gtatctccag 420 gccgactaca attacatcag tgccatcgag gctggggcat tcagcaaact taacaagctc 480 aaagtgctca tcctgaatga caaccttctg ctttcactgc ccagcaatgt gttccgcttt 540 gtcctgctga cccacttaga cctcaggggg aataggctaa aagtaatgcc ttttgctggc 600 gtccttgaac atattggagg gatcatggag attcagctgg aggaaaatcc atggaattgc 660 acttgtgact tacttcctct caaggcctgg ctagacacca taactgtttt tgtgggagag 720 attgtctgtg agactccctt taggttgcat gggaaagacg tgacccagct gaccaggcaa 780 gacctctgtc ccagaaaaag tgccagtgat tccagtcaga ggggcagcca tgctgacacc 840 cacgtccaaa ggctgtcacc tacaatgaat cctgctctca acccaaccag ggctccgaaa 900 gccagccggc cgcccaaaat gagaaatcgt ccaactcctc gagtgactgt gtcaaaggac 960 aggcaaagtt ttggacccat catggtgtac cagaccaagt ctcctgtgcc tctcacctgt 1020 cccagcagct gtgtctgcac ctctcagagc tcagacaatg gtctgaatgt aaactgccaa 1080 gaaaggaagt tcactaatat ctctgacctg cagcccaaac cgaccagtcc aaagaaactc 1140 tacctaacag ggaactatct tcaaactgtc tataagaatg acctcttaga atacagttct 1200 ttggacttac tgcacttagg aaacaacagg attgcagtca ttcaggaagg tgcctttaca 1260 aacctgacca gtttacgcag actttatctg aatggcaatt accttgaagt gctgtaccct 1320 tctatgtttg atggactgca gagcttgcaa tatctctatt tagagtataa tgtcattaag 1380 gaaattaagc ctctgacctt tgatgctttg attaacctac agctactgtt tctgaacaac 1440 aaccttcttc ggtccttacc tgataatata tttgggggga cggccctaac caggctgaat 1500 ctgagaaaca accatttttc tcacctgccc gtgaaagggg ttctggatca gctcccggct 1560 ttcatccaga tagatctgca ggagaacccc tgggactgta cctgtgacat catggggctg 1620 aaagactgga cagaacatgc caattcccct gtcatcatta atgaggtgac ttgcgaatct 1680 cctgctaagc atgcagggga gatactaaaa tttctgggga gggaggctat ctgtccagac 1740 agcccaaact tgtcagatgg aaccgtcttg tcaatgaatc acaatacaga cacacctcgg 1800 tcgcttagtg tgtctcctag ttcctatcct gaactacaca ctgaagttcc actgtctgtc 1860 ttaattctgg gattgcttgt tgttttcatc ttatctgtct gttttggggc tggtttattc 1920 gtctttgtct tgaaacgccg aaagggagtg ccgagcgttc ccaggaatac caacaactta 1980 gacgtaagct cctttcaatt acagtatggg tcttacaaca ctgagactca cgataaaaca 2040 gacggccatg tctacaacta tatcccccca cctgtgggtc agatgtgcca aaaccccatc 2100 tacatgcaga aggaaggaga cccagtagcc tattaccgaa acctgcaaga gttcagctat 2160 agcaacctgg aggagaaaaa agaagagcca gccacacctg cttacacaat aagtgccact 2220 gagctgctag aaaagcaggc cacaccaaga gagcctgagc tgctgtatca aaatattgct 2280 gagcgagtca aggaacttcc cagcgcaggc ctagtccact ataacttttg taccttacct 2340 aaaaggcagt ttgccccttc ctatgaatct cgacgccaaa accaagacag aatcaataaa 2400 accgttttat atggaactcc caggaaatgc tttgtggggc agtcaaaacc caaccaccct 2460 ttactgcaag ctaagccgca atcagaaccg gactacctcg aagttctgga aaaacaaact 2520 gcaatcagtc agctgtga 2538 21 1050 DNA Homo sapiens 21 atggggatca cctgctggat cgccctgtat gctgtggagg ccctccccac ctgccctttc 60 tcctgcaagt gtgacagccg cagcctggag gtggactgca gtggccttgg cctcaccacg 120 gtgcccccag acgtgcccgc agccacccga accctcttgc tcttgaacaa taagctgagt 180 gccctgccaa gctgggcttt cgccaacctc tccagcctgc agcggttgga cctgtccaac 240 aacttcctgg accggctgcc ccgctccatt ttcggggacc tgacgaatct gactgagctt 300 cagctgcgca ataacagcat caggaccctg gacagggacc tgctgcggca ctcgccgctg 360 ctccgccacc tggacctgtc catcaacggc ctggcccagt tgccccctgg tcttttcgac 420 gggctcctgg ctctgcgctc cctctcgctt cgctccaacc gtctgcagaa tctggaccgg 480 ctgacatttg aacccctagc aaacctgcag ctgctgcagg tcggggataa cccctgggag 540 tgtgactgta acctgcgtga gttcaaacac tggatggagt ggttctccta ccgaggggga 600 cgcttggacc agcttgcctg caccctgccc aaggagctga gggggaagga catgcggatg 660 gtccccatgg agatgttcaa ctactgctcc cagctggagg acgagaatag ctcagctggg 720 ctggatattc ctgggccacc ctgcaccaag gccagtccag agcctgctaa gcccaagccc 780 ggggctgagc cggagccgga gcccagcaca gcctgcccac agaagcagag gcaccggccg 840 gcgagcgtga ggcgagccat gggcacggtg atcattgcag gggtcgtgtg cggcgtcgtc 900 tgcatcatga tggtggtggc cgctgcctat ggctgcatct acgcctccct catggccaag 960 taccaccggg agctcaaaaa gcgccagccc ctgatggggg accccgaggg cgagcacgag 1020 gaccagaagc agatctcttc tgtggcctga 1050 22 2215 DNA Homo sapiens 22 atgggaatga ctgttataaa gcaaatcaca gatgacctat ttgtatggaa tgttctgaat 60 cgcgaagaag taaacatcat ttgctgcgag aaggtggagc aggatgctgc tagagggatc 120 attcacatga ttttgaaaaa gggttcagag tcctgtaacc tctttcttaa atcccttaag 180 gagtggaact atcctctatt tcaggacttg aatggacaaa gtctttttca tcagacatca 240 gaaggagact tggacgattt ggctcaggat ttaaaggact tgtaccatac cccatctttt 300 ctgaactttt atccccttgg tgaagatatt gacattattt ttaacttgaa aagcaccttc 360 acagaacctg tcctgtggag gaaggaccaa caccatcacc gcgtggagca gctgaccctg 420 aatggcctcc tgcaggctct tcagagcccc tgcatcattg aaggggaatc tggcaaaggc 480 aagtccactc tgctgcagcg aattgccatg ctctggggct ccggaaagtg caaggctctg 540 accaagttca aattcgtctt cttcctccgt ctcagcaggg cccagggtgg actttttgaa 600 accctctgtg atcaactcct ggatatacct ggcacaatca ggaagcagac attcatggcc 660 atgctgctga agctgcggca gagggttctt ttccttcttg atggctacaa tgaattcaag 720 ccccagaact gcccagaaat cgaagccctg ataaaggaaa accaccgctt caagaacatg 780 gtcatcgtca ccactaccac tgagtgcctg aggcacatac ggcagtttgg tgccctgact 840 gctgaggtgg gggatatgac agaagacagc gcccaggctc tcatccgaga agtgctgatc 900 aaggagcttg ctgaaggctt gttgctccaa attcagaaat ccaggtgctt gaggaatctc 960 atgaagaccc ctctctttgt ggtcatcact tgtgcaatcc agatgggtga aagtgagttc 1020 cactctcaca cacaaacaac gctgttccat accttctatg atctgttgat acagaaaaac 1080 aaacacaaac ataaaggtgt ggctgcaagt gacttcattc ggagcctgga ccactgtgga 1140 gacctagctc tggagggtgt gttctcccac aagtttgatt tcgaactgca ggatgtgtcc 1200 agcgtgaatg aggatgtcct gctgacaact gggctcctct gtaaatatac agctcaaagg 1260 ttcaagccaa agtataaatt ctttcacaag tcattccagg agtacacagc aggacgaaga 1320 ctcagcagtt tattgacgtc tcatgagcca gaggaggtga ccaaggggaa tggttacttg 1380 cagaaaatgg tttccatttc ggacattaca tccacttata gcagcctgct ccggtacacc 1440 tgtgggtcat ctgtggaagc caccagggct gttatgaagc acctcgcagc agtgtatcaa 1500 cacggctgcc ttctcggact ttccatcgcc aagaggcctc tctggagaca ggaatctttg 1560 caaagtgtga aaaacaccac tgagcaagaa attctgaaag ccataaacat caattccttt 1620 gtagagtgtg gcatccattt atatcaagag agtacatcca aatcagccct gagccaagaa 1680 tttgaagctt tctttcaagg taaaagctta tatatcaact cagggaacat ccccgattac 1740 ttatttgact tctttgaaca tttgcccaat tgtgcaagtg ccctggactt cattaaactg 1800 gacttttatg ggggagctat ggcttcatgg gaaaaggctg cagaagacac aggtggaatc 1860 cacatggaag aggccccaga aacctacatt cccagcaggg ctgtatcttt gttcttcaac 1920 tggaagcagg aattcaggac tctggaggtc acactccggg atttcagcaa gttgaataag 1980 caagatatca gatatctggg gaaaatattc agctctgcca caagcctcag gctgcaaata 2040 aagagatgtg ctggtgtggc tggaagcctc agtttggtcc tcagcacctg taagaacatt 2100 tattctctca tggtggaagc cagtcccctc accatagaag atgagaggca catcacatct 2160 gtaacaaacc tgaaaacctt gagtattcat gacctacaga atcaacggct gccgg 2215 23 3213 DNA Homo sapiens 23 atgtacaaaa gccttaacat tgacgagtgt gatttgcatg cctggctgga tttgcctgcc 60 gagaaacctt taggggtggt taatcgggtc tgctggggct tcatcaggtt caaggggtac 120 atgtacccct tggactactt gaatttcata aaggacaata gccgagccct tattcaaaga 180 atgggaatga ctgttataaa gcaaatcaca gatgacctat ttgtatggaa tgttctgaat 240 cgcgaagaag taaacatcat ttgctgcgag aaggtggagc aggatgctgc tagagggatc 300 attcacatga ttttgaaaaa gggttcagag tcctgtaacc tctttcttaa atcccttaag 360 gagtggaact atcctctatt tcaggacttg aatggacaaa gtctttttca tcagacatca 420 gaaggagact tggacgattt ggctcaggat ttaaaggact tgtaccatac cccatctttt 480 ctgaactttt atccccttgg tgaagatatt gacattattt ttaacttgaa aagcaccttc 540 acagaacctg tcctgtggag gaaggaccaa caccatcacc gcgtggagca gctgaccctg 600 aatggcctcc tgcaggctct tcagagcccc tgcatcattg aaggggaatc tggcaaaggc 660 aagtccactc tgctgcagcg aattgccatg ctctggggct ccggaaagtg caaggctctg 720 accaagttca aattcgtctt cttcctccgt ctcagcaggg cccagggtgg actttttgaa 780 accctctgtg atcaactcct ggatatacct ggcacaatca ggaagcagac attcatggcc 840 atgctgctga agctgcggca gagggttctt ttccttcttg atggctacaa tgaattcaag 900 ccccagaact gcccagaaat cgaagccctg ataaaggaaa accaccgctt caagaacatg 960 gtcatcgtca ccactaccac tgagtgcctg aggcacatac ggcagtttgg tgccctgact 1020 gctgaggtgg gggatatgac agaagacagc gcccaggctc tcatccgaga agtgctgatc 1080 aaggagcttg ctgaaggctt gttgctccaa attcagaaat ccaggtgctt gaggaatctc 1140 atgaagaccc ctctctttgt ggtcatcact tgtgcaatcc agatgggtga aagtgagttc 1200 cactctcaca cacaaacaac gctgttccat accttctatg atctgttgat acagaaaaac 1260 aaacacaaac ataaaggtgt ggctgcaagt gacttcattc ggagcctgga ccactgtgga 1320 gacctagctc tggagggtgt gttctcccac aagtttgatt tcgaactgca ggatgtgtcc 1380 agcgtgaatg aggatgtcct gctgacaact gggctcctct gtaaatatac agctcaaagg 1440 ttcaagccaa agtataaatt ctttcacaag tcattccagg agtacacagc aggacgaaga 1500 ctcagcagtt tattgacgtc tcatgagcca gaggaggtga ccaaggggaa tggttacttg 1560 cagaaaatgg tttccatttc ggacattaca tccacttata gcagcctgct ccggtacacc 1620 tgtgggtcat ctgtggaagc caccagggct gttatgaagc acctcgcagc agtgtatcaa 1680 cacggctgcc ttctcggact ttccatcgcc aagaggcctc tctggagaca ggaatctttg 1740 caaagtgtga aaaacaccac tgagcaagaa attctgaaag ccataaacat caattccttt 1800 gtagagtgtg gcatccattt atatcaagag agtacatcca aatcagccct gagccaagaa 1860 tttgaagctt tctttcaagg taaaagctta tatatcaact cagggaacat ccccgattac 1920 ttatttgact tctttgaaca tttgcccaat tgtgcaagtg ccctggactt cattaaactg 1980 gacttttatg ggggagctat ggcttcatgg gaaaaggctg cagaagacac aggtggaatc 2040 cacatggaag aggccccaga aacctacatt cccagcaggg ctgtatcttt gttcttcaac 2100 tggaagcagg aattcaggac tctggaggtc acactccggg atttcagcaa gttgaataag 2160 caagatatca gatatctggg gaaaatattc agctctgcca caagcctcag gctgcaaata 2220 aagagatgtg ctggtgtggc tggaagcctc agtttggtcc tcagcacctg taagaacatt 2280 tattctctca tggtggaagc cagtcccctc accatagaag atgagaggca catcacatct 2340 gtaacaaacc tgaaaacctt gagtattcat gacctacaga atcaacggct gccgggtggt 2400 ctgactgaca gcttgggtaa cttgaagaac cttacaaagc tcataatgga taacataaag 2460 atgaatgaag aagatgctat aaaactagct gaaggcctga aaaacctgaa gaagatgtgt 2520 ttatttcatt tgacccactt gtctgacatt ggagagggaa tggattacat agtcaagtct 2580 ctgtcaagtg aaccctgtga ccttgaagaa attcaattag tctcctgctg cttgtctgca 2640 aatgcagtga aaatcctagc tcagaatctt cacaatttgg tcaaactgag cattcttgat 2700 ttatcagaaa attacctgga aaaagatgga aatgaagctc ttcatgaact gatcgacagg 2760 atgaacgtgc tagaacagct caccgcactg atgctgccct ggggctgtga cgtgcaaggc 2820 agcctgagca gcctgttgaa acatttggag gaggtcccac aactcgtcaa gcttgggttg 2880 aaaaactgga gactcacaga tacagagatt agaattttag gtgcattttt tggaaagaac 2940 cctctgaaaa acttccagca gttgaatttg gcgggaaatc gtgtgagcag tgatggatgg 3000 cttgccttca tgggtgtatt tgagaatctt aagcaattag tgttttttga ctttagtact 3060 aaagaatttc tacctgatcc agcattagtc agaaaactta gccaagtgtt atccaagtta 3120 acttttctgc aagaagctag gcttgttggg tggcaatttg atgatgatga tctcagtgtt 3180 attacaggtg cttttaaact agtaactgct taa 3213 24 1464 DNA Homo sapiens 24 atgccgcctt tgccacagtg gtcctttcct cgtccagacc actgccatgt gactttcgtg 60 accctcaagt gtgactcctc caagaagagg cgccgtggcc gcaagtcccc atccaaggag 120 gtgtcccaca tcacagcaga gtttgagatc gagacaaaga tggaagaggc ctcagacaca 180 tgcgaagcgg actgcttgcg gaagcgagca gaacagagcc tgcaggccgc catcaagacc 240 ctgcgcaagt ccatcggccg gcagcagttc tatgtccagg tctcaggcac tgagtacgag 300 gtagcccaga ggccagccaa ggcgctggag gggcaggggg catgtggcgc aggccaggtg 360 ctacaggaca gcaaatgcgt tgcctgtggg cctggcaccc acttcggtgg tgagctcggc 420 cagtgtgtgt catgtatgcc aggaacatac caggacatgg aaggccagct cagttgcaca 480 ccgtgcccca gcagcgacgg gcttggtctg cctggtgccc gcaacgtgtc ggaatgtgga 540 ggcaagtgcg ggcctagaag gagaggcttc ttctcggccg atggcttcaa gccctgccag 600 gcctgccccg tgggcacgta ccagcctgag cccgggcgca ccggctgctt cccctgtgga 660 gggggtttgc tcaccaaaca cgaaggcacc acctccttcc aggactgcga ggctaaagtg 720 cactgctccc ccggccacca ctacaacacc accacccacc gctgcatccg ctgccccgtc 780 ggcacctacc agcccgagtt tggccagaac cactgcatca cctgtccggg caacaccagc 840 acagacttcg atggctccac caacgtcaca cactgcaaaa accagcactg cggcggcgag 900 cttggtgact acaccggcta catcgagtcc cccaactacc ctggcgacta cccagccaac 960 gctgaatgcg tctggcacat cgcgcctccc ccaaagcgca ggatcctcat cgtggtccct 1020 gagatcttcc tgcccatcga ggatgagtgc ggcgatgttc tggtcatgag gaagagtgcc 1080 tctcccacgt ccatcaccac ctatgagacc tgccagacct acgagaggcc catcgccttc 1140 acctcccgct cccgcaagct ctggatccag ttcaaatcca atgaaggcaa cagcggcaaa 1200 ggcttccaag tgccctatgt cacctacgat gaggactacc agcaactcat agaggacatc 1260 gtgcgcgatg ggcgcctgta cgcctcggag aaccaccagg aaattttgaa agacaagaag 1320 ctgatcaagg ccctcttcga cgtgctggcg catccccaga actacttcaa gtacacagcc 1380 caggaatcca aggagatgtt cccacggtcc ttcatcaaac tgctgcgctc caaagtgtct 1440 cggttcctgc ggccctacaa ataa 1464 25 2897 DNA Homo sapiens 25 atgggcgcgg cggccgtgcg ctggcacttg tgcgtgctgc tggccctggg cacacgcggg 60 cggctggccg ggggcagcgg gctcccaggt tcagtcgacg tggatgagtg ctcagagggc 120 acagatgact gccacatcga tgccatctgt cagaacacgc ccaagtccta caaatgcctc 180 tgcaagccag gctacaaggg ggaaggcaag cagtgtgaag acattgacga gtgtgagaat 240 gactactaca atgggggctg tgtccacgag tgcatcaaca tcccggggaa ctacaggtgt 300 acctgctttg atggcttcat gctggcacac gatggacaca actgcctgga tgtggacgag 360 tgtcaggaca ataatggtgg ctgccagcag atctgcgtca atgccatggg cagctacgag 420 tgtcagtgcc acagtggctt cttccttagt gacaaccagc atacctgcat ccaccgctcc 480 aatgagggta tgaactgcat gaacaaagac catggctgtg cccacatctg ccgggagacg 540 cccaaaggtg gggtggcctg cgactgcagg cccggctttg accttgccca aaaccagaag 600 gactgcacac taacctgtaa ttatggaaac ggaggctgcc agcacagctg tgaggacaca 660 gacacaggcc ccacgtgtgg ttgccaccag aagtacgccc tccactcaga cggtcgcacg 720 tgcatcgaga cgtgcgcagt caataacgga ggctgcgacc ggacatgcaa ggacacagcc 780 actggcgtgc gatgcagctg ccccgttgga ttcacactgc agccggacgg gaagacatgc 840 aaagacatca acgagtgcct ggtcaacaac ggaggctgcg accacttctg ccgcaacacc 900 gtgggcagct tcgagtgcgg ctgccggaag ggctacaagc tgctcaccga cgagcgcacc 960 tgccaggaca tcgacgagtg ctccttcgag cggacctgtg accacatctg catcaactcc 1020 ccgggcagct tccagtgcct gtgtcaccgc ggctacatcc tctacgggac aacccactgc 1080 ggagatgtgg acgagtgcag catgagcaac gggagctgtg accagggctg cgtcaacacc 1140 aagggcagct acgagtgcgt ctgtcccccg gggaggcggc tccactggaa cgggaaggat 1200 tgcgtggaga caggcaagtg tctttctcgc gccaagacct ccccccgggc ccagctgtcc 1260 tgcagcaagg caggcggtgt ggagagctgc ttcctttcct gcccggctca cacactcttc 1320 gtgccagact cggaaaatag ctacgtcctg agctgcggag ttccagggcc gcagggcaag 1380 gcgctgcaga aacgcaacgg caccagctct ggcctcgggc ccagctgctc agatgccccc 1440 accaccccca tcaaacagaa ggcccgcttc aagatccgag atgccaagtg ccacctccgg 1500 ccccacagcc aggcacgagc aaaggagacc gccaggcagc cgctgctgga ccactgccat 1560 gtgactttcg tgaccctcaa gtgtgactcc tccaagaaga ggcgccgtgg ccgcaagtcc 1620 ccatccaagg aggtgtccca catcacagca gagtttgaga tcgagacaaa gatggaagag 1680 gcctcagaca catgcgaagc ggactgcttg cggaagcgag cagaacagag cctgcaggcc 1740 gccatcaaga ccctgcgcaa gtccatcggc cggcagcagt tctatgtcca ggtctcaggc 1800 actgagtacg aggtagccca gaggccagcc aaggcgctgg aggggcaggg ggcatgtggc 1860 gcaggccagg tgctacagga cagcaaatgc gttgcctgtg ggcctggcac ccacttcggt 1920 ggtgagctcg gccagtgtgt gtcatgtatg ccaggaacat accaggacat ggaaggccag 1980 ctcagttgca caccgtgccc cagcagcgac gggcttggtc tgcctggtgc ccgcaacgtg 2040 tcggaatgtg gaggccagtg ttctccaggc ttcttctcgg ccgatggctt caagccctgc 2100 caggcctgcc ccgtgggcac gtaccagcct gagcccgggc gcaccggctg cttcccctgt 2160 ggagggggtt tgctcaccaa acacgaaggc accacctcct tccaggactg cgaggctaaa 2220 gtgcactgct cccccggcca ccactacaac accaccaccc accgctgcat ccgctgcccc 2280 gtcggcacct accagcccga gtttggccag aaccactgca tcacctgtcc gggcaacacc 2340 agcacagact tcgatggctc caccaacgtc acacactgca aaaaccagca ctgcggcggc 2400 gagcttggtg actacaccgg ctacatcgag tcccccaact accctggcga ctacccagcc 2460 aacgctgaat gcgtctggca catcgcgcct cccccaaagc gcaggatcct catcgtggtc 2520 cctgagatct tcctgcccat cgaggatgag tgcggcgatg ttctggtcat gaggaagagt 2580 gcctctccca cgtccatcac cacctatgag acctgccaga cctacgagag gcccatcgcc 2640 ttcacctccc gctcccgcaa gctctggatc cagttcaaat ccaatgaagg caacagcggc 2700 aaaggcttcc aagtgcccta tgtcacctac gatggtaaga tccactgtct tcacggccca 2760 ctgtgcacgg ctcaggcggg gccctggaga cacagagatg agtcgcacgt ccccgccccc 2820 tcagggagct gcgacctggc aggtacagac ctggaagcag aacgaacact gtcaggggcc 2880 agagccagac aggctga 2897 26 2151 DNA Homo sapiens 26 atggctagga tgagctttgt tatagcagct tgccaattgg tgctgggcct actaatgact 60 tcattaaccg agtcttccat acagaatagt gagtgtccac aactttgcgt atgtgaaatt 120 cgtccctggt ttaccccaca gtcaacttac agagaagcca ccactgttga ttgcaatgac 180 ctccgcttaa caaggattcc cagtaacctc tctagtgaca cacaagtgct tctcttacag 240 agcaataaca tcgcaaagac tgtggatgag ctgcagcagc ttttcaactt gactgaacta 300 gatttctccc aaaacaactt tactaacatt aaggaggtcg ggctggcaaa cctaacccag 360 ctcacaacgc tgcatttgga ggaaaatcag attaccgaga tgactgatta ctgtctacaa 420 gacctcagca accttcaaga actctacatc aaccacaacc aaattagcac tatttctgct 480 catgcttttg caggcttaaa aaatctatta aggctccacc tgaactccaa caaattgaaa 540 gttattgata gtcgctggtt tgattctaca cccaacctgg aaattctcat gatcggagaa 600 aaccctgtga ttggaattct ggatatgaac ttcaaacccc tcgcaaattt gagaagctta 660 gttttggcag gaatgtatct cactgatatt cctggaaatg ctttggtggg tctggatagc 720 cttgagagcc tgtcttttta tgataacaaa ctggttaaag tccctcaact tgccctgcaa 780 aaagttccaa atttgaaatt cttagacctc aacaaaaacc ccattcacaa aatccaagaa 840 ggggacttca aaaatatgct tcggttaaaa gaactgggaa tcaacaatat gggcgagctc 900 gtttctgtcg accgctatgc cctggataac ttgcctgaac tcacaaagct ggaagccacc 960 aataacccta aactctctta catccaccgc ttggctttcc gaagtgtccc tgctctggaa 1020 agcttgatgc tgaacaacaa tgccttgaat gccatttacc aaaagacagt cgaatccctc 1080 cccaatctgc gtgagatcag tatccatagc aatcccctca ggtgtgactg tgtgatccac 1140 tggattaact ccaacaaaac caacatccgc ttcatggagc ccctgtccat gttctgtgcc 1200 atgccgcccg aatataaagg gcaccaggtg aaggaagttt taatccagga ttcgagtgaa 1260 cagtgcctcc caatgatatc tcacgacagc ttcccaaatc gtttaaacgt ggatatcggc 1320 acgacggttt tcctagactg tcgagccatg gctgagccag aacctgaaat ttactgggtc 1380 actcccattg gaaataagat aactgtggaa accctttcag ataaatacaa gctaagtagc 1440 gaaggtacct tggaaatatc taacatacaa attgaagact caggaagata cacatgtgtt 1500 gcccagaatg tccaaggggc agacactcgg gtggcaacaa ttaaggttaa tgggaccctt 1560 ctggatggta cccaggtgct aaaaatatac gtcaagcaga cagaatccca ttccatctta 1620 gtgtcctgga aagttaattc caatgtcatg acgtcaaact taaaatggtc gtctgccacc 1680 atgaagattg ataaccctca cataacatat actgccaggg tcccagtcga tgtccatgaa 1740 tacaacctaa cgcatctgca gccttccaca gattatgaag tgtgtctcac agtgtccaat 1800 attcatcagc agactcaaaa gtcatgcgta aatgtcacaa ccaaaaatgc cgccttcgca 1860 gtggacatct ctgatcaaga aaccagtaca gcccttgctg cagtaatggg gtctatgttt 1920 gccgtcatta gccttgcgtc cattgctgtg tactttgcca aaagatttaa gagaaaaaac 1980 taccaccact cattaaaaaa gtatatgcaa aaaacctctt caatcccact aaatgagctg 2040 tacccaccac tcattaacct ctgggaaggt gacagcgaga aagacaaaga tggttctgca 2100 gacaccaagc caacccaggt cgacacatcc agaagctatt acatgtggta a 2151 27 766 PRT Homo sapiens 27 Met Glu Lys Val Leu Phe Tyr Leu Phe Leu Ile Gly Ile Ala Val Lys 1 5 10 15 Ala Gln Ile Cys Pro Lys Arg Cys Val Cys Gln Ile Leu Ser Pro Asn 20 25 30 Leu Ala Thr Leu Cys Ala Lys Lys Gly Leu Leu Phe Val Pro Pro Asn 35 40 45 Ile Asp Arg Arg Thr Val Glu Leu Arg Leu Ala Asp Asn Phe Val Thr 50 55 60 Asn Ile Lys Arg Lys Asp Phe Ala Asn Met Thr Ser Leu Val Asp Leu 65 70 75 80 Thr Leu Ser Arg Asn Thr Ile Ser Phe Ile Thr Pro His Ala Phe Ala 85 90 95 Asp Leu Arg Asn Leu Arg Ala Leu His Leu Asn Ser Asn Arg Leu Thr 100 105 110 Lys Ile Thr Asn Asp Met Phe Ser Gly Leu Ser Asn Leu His His Leu 115 120 125 Ile Leu Asn Asn Asn Gln Leu Thr Leu Ile Ser Ser Thr Ala Phe Asp 130 135 140 Asp Val Phe Ala Leu Glu Glu Leu Asp Leu Ser Tyr Asn Asn Leu Glu 145 150 155 160 Thr Ile Pro Trp Asp Ala Val Glu Lys Met Val Ser Leu His Thr Leu 165 170 175 Ser Leu Asp His Asn Met Ile Asp Asn Ile Pro Lys Gly Thr Phe Ser 180 185 190 His Leu His Lys Met Thr Arg Leu Asp Val Thr Ser Asn Lys Leu Gln 195 200 205 Lys Leu Pro Pro Asp Pro Leu Phe Gln Arg Ala Gln Val Leu Ala Thr 210 215 220 Ser Gly Ile Ile Ser Pro Ser Thr Phe Ala Leu Ser Phe Gly Gly Asn 225 230 235 240 Pro Leu His Cys Asn Cys Glu Leu Leu Trp Leu Arg Arg Leu Ser Arg 245 250 255 Glu Asp Asp Leu Glu Thr Cys Ala Ser Pro Pro Leu Leu Thr Gly Arg 260 265 270 Tyr Phe Trp Ser Ile Pro Glu Glu Glu Phe Leu Cys Glu Pro Pro Leu 275 280 285 Ile Thr Arg His Thr His Glu Met Arg Val Leu Glu Gly Gln Arg Ala 290 295 300 Thr Leu Arg Cys Lys Ala Arg Gly Asp Pro Glu Pro Ala Ile His Trp 305 310 315 320 Ile Ser Pro Glu Gly Lys Leu Ile Ser Asn Ala Thr Arg Ser Leu Val 325 330 335 Tyr Asp Asn Gly Thr Leu Asp Ile Leu Ile Thr Thr Val Lys Asp Thr 340 345 350 Gly Ala Phe Thr Cys Ile Ala Ser Asn Pro Ala Gly Glu Ala Thr Gln 355 360 365 Ile Val Asp Leu His Ile Ile Lys Leu Pro His Leu Leu Asn Ser Thr 370 375 380 Asn His Ile His Glu Pro Asp Pro Gly Ser Ser Asp Ile Ser Thr Ser 385 390 395 400 Thr Lys Ser Gly Ser Asn Thr Ser Ser Ser Asn Gly Asp Thr Lys Leu 405 410 415 Ser Gln Asp Lys Ile Val Val Ala Glu Ala Thr Ser Ser Thr Ala Leu 420 425 430 Leu Lys Phe Asn Phe Gln Arg Asn Ile Pro Gly Ile Arg Met Phe Gln 435 440 445 Ile Gln Tyr Asn Gly Thr Tyr Asp Asp Thr Leu Val Tyr Arg Met Ile 450 455 460 Pro Pro Thr Ser Lys Thr Phe Leu Val Asn Asn Leu Ala Ala Gly Thr 465 470 475 480 Met Tyr Asp Leu Cys Val Leu Ala Ile Tyr Asp Asp Gly Ile Thr Ser 485 490 495 Leu Thr Ala Thr Arg Val Val Gly Cys Ile Gln Phe Thr Thr Glu Gln 500 505 510 Asp Tyr Val Arg Cys His Phe Met Gln Ser Gln Phe Leu Gly Gly Thr 515 520 525 Met Ile Ile Ile Ile Gly Gly Ile Ile Val Ala Ser Val Leu Val Phe 530 535 540 Ile Ile Ile Leu Met Ile Arg Tyr Lys Val Cys Asn Asn Asn Gly Gln 545 550 555 560 His Lys Val Thr Lys Val Ser Asn Val Tyr Ser Gln Thr Asn Gly Ala 565 570 575 Gln Ile Gln Gly Cys Ser Val Thr Leu Pro Gln Ser Val Ser Lys Gln 580 585 590 Ala Val Gly His Glu Glu Asn Ala Gln Cys Cys Lys Ala Thr Ser Asp 595 600 605 Asn Val Ile Gln Ser Ser Glu Thr Cys Ser Ser Gln Asp Ser Ser Thr 610 615 620 Thr Thr Ser Ala Leu Pro Pro Ser Trp Thr Ser Ser Thr Ser Val Ser 625 630 635 640 Gln Lys Gln Lys Arg Lys Thr Gly Thr Lys Pro Ser Thr Glu Pro Gln 645 650 655 Asn Glu Ala Val Thr Asn Val Glu Ser Gln Asn Thr Asn Arg Asn Asn 660 665 670 Ser Thr Ala Leu Gln Leu Ala Ser Arg Pro Pro Asp Ser Val Thr Glu 675 680 685 Gly Pro Thr Ser Lys Arg Ala His Ile Lys Pro Ser Lys Phe Ile Thr 690 695 700 Leu Pro Ala Glu Arg Ser Gly Ala Arg His Lys Tyr Ser Leu Asn Gly 705 710 715 720 Glu Leu Lys Glu Tyr Tyr Cys Tyr Ile Asn Ser Pro Asn Thr Cys Gly 725 730 735 Leu Phe Pro Lys Arg Ser Met Ser Met Asn Val Met Phe Ile Gln Ser 740 745 750 Asp Cys Ser Asp Gly His Ser Gly Lys Ala Thr Leu Lys Phe 755 760 765 28 148 PRT Homo sapiens 28 Ala Met Leu Gly Leu Pro Trp Lys Gly Gly Leu Ser Trp Ala Leu Leu 1 5 10 15 Leu Leu Leu Leu Gly Ser Gln Ile Leu Leu Ile Tyr Ala Trp His Phe 20 25 30 His Glu Gln Arg Asp Cys Asp Glu His Asn Val Met Ala Arg Tyr Leu 35 40 45 Pro Ala Thr Val Glu Phe Ala Val His Thr Phe Asn Gln Gln Ser Lys 50 55 60 Asp Tyr Tyr Ala Tyr Arg Leu Gly His Ile Leu Asn Ser Trp Lys Glu 65 70 75 80 Gln Val Glu Ser Lys Thr Val Phe Ser Met Glu Leu Leu Leu Gly Arg 85 90 95 Thr Arg Cys Gly Lys Phe Glu Asp Asp Ile Asp Asn Cys His Phe Gln 100 105 110 Glu Ser Thr Glu Leu Asn Asn Thr Phe Thr Cys Phe Phe Thr Ile Ser 115 120 125 Thr Arg Pro Trp Met Thr Gln Phe Ser Leu Leu Asn Lys Thr Cys Leu 130 135 140 Glu Gly Phe His 145 29 159 PRT Homo sapiens 29 Asx Met Trp Ser Leu Pro Pro Ser Arg Ala Leu Ser Cys Ala Pro Leu 1 5 10 15 Leu Leu Leu Phe Ser Phe Gln Phe Leu Val Thr Tyr Ala Trp Arg Phe 20 25 30 Gln Glu Glu Glu Glu Trp Asn Asp Gln Lys Gln Ile Ala Val Tyr Leu 35 40 45 Pro Pro Thr Leu Glu Phe Ala Val Tyr Thr Phe Asn Lys Gln Ser Lys 50 55 60 Asp Trp Tyr Ala Tyr Lys Leu Val Pro Val Leu Ala Ser Trp Lys Glu 65 70 75 80 Gln Gly Tyr Asp Lys Met Thr Phe Ser Met Asn Leu Gln Leu Gly Arg 85 90 95 Thr Met Cys Gly Lys Phe Glu Asp Asp Ile Asp Asn Cys Pro Phe Gln 100 105 110 Glu Ser Pro Glu Leu Asn Asn Val Arg Gln Asp Thr Ser Phe Pro Pro 115 120 125 Gly Tyr Ser Cys Gly Cys Arg Met Gly Cys Gly Ala Asp Thr Asp Leu 130 135 140 His Leu Leu Leu His His Trp Asn Arg Ala Leu Glu Asp Thr Val 145 150 155 30 148 PRT Homo sapiens 30 Asx Met Trp Ser Leu Pro Pro Ser Arg Ala Leu Ser Cys Ala Pro Leu 1 5 10 15 Leu Leu Leu Phe Ser Phe Gln Phe Leu Val Thr Tyr Ala Trp Arg Phe 20 25 30 Gln Glu Glu Glu Glu Trp Asn Asp Gln Lys Gln Ile Ala Val Tyr Leu 35 40 45 Pro Pro Thr Leu Glu Phe Ala Val Tyr Thr Phe Asn Lys Gln Ser Lys 50 55 60 Asp Trp Tyr Ala Tyr Lys Leu Val Pro Val Leu Ala Ser Trp Lys Glu 65 70 75 80 Gln Gly Tyr Asp Lys Met Thr Phe Ser Met Asn Leu Gln Leu Gly Arg 85 90 95 Thr Met Cys Gly Lys Phe Glu Asp Asp Ile Asp Asn Cys Pro Phe Gln 100 105 110 Glu Ser Pro Glu Leu Asn Asn Thr Cys Thr Cys Phe Phe Thr Ile Gly 115 120 125 Ile Glu Pro Trp Arg Thr Arg Phe Asp Leu Trp Asn Lys Thr Cys Ser 130 135 140 Gly Gly His Ser 145 31 820 PRT Homo sapiens 31 Met Leu Arg Leu Gly Leu Cys Ala Ala Ala Leu Leu Cys Val Cys Arg 1 5 10 15 Pro Gly Ala Val Arg Ala Asp Cys Trp Leu Ile Glu Gly Asp Lys Gly 20 25 30 Tyr Val Trp Leu Ala Ile Cys Ser Gln Asn Gln Pro Pro Tyr Glu Thr 35 40 45 Ile Pro Gln His Ile Asn Ser Thr Val His Asp Leu Arg Leu Asn Glu 50 55 60 Asn Lys Leu Lys Ala Val Leu Tyr Ser Ser Leu Asn Arg Phe Gly Asn 65 70 75 80 Leu Thr Asp Leu Asn Leu Thr Lys Asn Glu Ile Ser Tyr Ile Glu Asp 85 90 95 Gly Ala Phe Leu Gly Gln Ser Ser Leu Gln Val Leu Gln Leu Gly Tyr 100 105 110 Asn Lys Leu Ser Asn Leu Thr Glu Gly Met Leu Arg Gly Met Ser Arg 115 120 125 Leu Gln Phe Leu Phe Val Gln His Asn Leu Ile Glu Val Val Thr Pro 130 135 140 Thr Ala Phe Ser Glu Cys Pro Ser Leu Ile Ser Ile Asp Leu Ser Ser 145 150 155 160 Asn Arg Leu Ser Arg Leu Asp Gly Ala Thr Phe Ala Ser Leu Ala Ser 165 170 175 Leu Met Val Cys Glu Leu Ala Gly Asn Pro Phe Asn Cys Glu Cys Asp 180 185 190 Leu Phe Gly Phe Leu Ala Trp Leu Val Val Phe Asn Asn Val Thr Lys 195 200 205 Asn Tyr Asp Arg Leu Gln Cys Glu Ser Pro Arg Glu Phe Ala Gly Tyr 210 215 220 Pro Leu Leu Val Pro Arg Pro Tyr His Ser Leu Asn Ala Ile Thr Val 225 230 235 240 Leu Gln Ala Lys Cys Arg Asn Gly Ser Leu Pro Ala Arg Pro Val Ser 245 250 255 His Pro Thr Pro Tyr Ser Thr Asp Ala Gln Arg Glu Pro Asp Glu Asn 260 265 270 Ser Gly Phe Asn Pro Asp Glu Ile Leu Ser Val Glu Pro Pro Ala Ser 275 280 285 Ser Thr Thr Asp Ala Ser Ala Gly Pro Ala Ile Lys Leu His His Val 290 295 300 Thr Phe Thr Ser Ala Thr Leu Val Val Ile Ile Pro His Pro Tyr Ser 305 310 315 320 Lys Met Tyr Ile Leu Val Gln Tyr Asn Asn Ser Tyr Phe Ser Asp Val 325 330 335 Met Thr Leu Lys Asn Lys Lys Glu Ile Val Thr Leu Asp Lys Leu Arg 340 345 350 Ala His Thr Glu Tyr Thr Phe Cys Val Thr Ser Leu Arg Asn Ser Arg 355 360 365 Arg Phe Asn His Thr Cys Leu Thr Phe Thr Thr Arg Asp Pro Val Pro 370 375 380 Gly Asp Leu Ala Pro Ser Thr Ser Thr Thr Thr His Tyr Ile Met Thr 385 390 395 400 Ile Leu Gly Cys Leu Phe Gly Met Val Ile Val Leu Gly Ala Val Tyr 405 410 415 Tyr Cys Leu Arg Lys Arg Arg Met Gln Glu Glu Lys Gln Lys Ser Val 420 425 430 Asn Val Lys Lys Thr Ile Leu Glu Met Arg Tyr Gly Ala Asp Val Asp 435 440 445 Ala Gly Ser Ile Val His Ala Ala Gln Lys Leu Gly Glu Pro Pro Val 450 455 460 Leu Pro Val Ser Arg Met Ala Ser Ile Pro Ser Met Ile Gly Glu Lys 465 470 475 480 Leu Pro Thr Ala Lys Gly Leu Glu Ala Gly Leu Asp Thr Pro Lys Val 485 490 495 Ala Thr Lys Gly Asn Tyr Ile Glu Val Arg Thr Gly Ala Gly Gly Asp 500 505 510 Gly Leu Ala Arg Pro Glu Asp Asp Leu Pro Asp Leu Glu Asn Gly Gln 515 520 525 Gly Ser Ala Ala Glu Ile Ser Thr Ile Ala Lys Glu Val Asp Lys Val 530 535 540 Asn Gln Ile Ile Asn Asn Cys Ile Asp Ala Leu Lys Leu Asp Ser Ala 545 550 555 560 Ser Phe Leu Gly Gly Gly Ser Ser Ser Gly Asp Pro Glu Leu Ala Phe 565 570 575 Glu Cys Gln Ser Leu Pro Ala Ala Ala Ala Ala Ser Ser Ala Thr Gly 580 585 590 Pro Gly Ala Leu Glu Arg Pro Ser Phe Leu Ser Pro Pro Tyr Lys Glu 595 600 605 Ser Ser His His Pro Leu Gln Arg Gln Leu Ser Ala Asp Ala Ala Val 610 615 620 Thr Arg Lys Thr Cys Ser Val Ser Ser Ser Gly Ser Ile Lys Ser Ala 625 630 635 640 Lys Val Phe Ser Leu Asp Val Pro Asp His Pro Ala Ala Thr Gly Leu 645 650 655 Ala Lys Gly Asp Ser Lys Tyr Ile Glu Lys Gly Ser Pro Leu Asn Ser 660 665 670 Pro Leu Asp Arg Leu Pro Leu Val Pro Ala Gly Ser Gly Gly Gly Ser 675 680 685 Gly Gly Gly Gly Gly Ile His His Leu Glu Val Lys Pro Ala Tyr His 690 695 700 Cys Ser Glu His Arg His Ser Phe Pro Ala Leu Tyr Tyr Glu Glu Gly 705 710 715 720 Ala Asp Ser Leu Ser Gln Arg Val Ser Phe Leu Lys Pro Leu Thr Arg 725 730 735 Ser Lys Arg Asp Ser Thr Tyr Ser Gln Leu Ser Pro Arg His Tyr Tyr 740 745 750 Ser Gly Tyr Ser Ser Ser Pro Glu Tyr Ser Ser Glu Ser Thr His Lys 755 760 765 Ile Trp Glu Arg Phe Arg Pro Tyr Lys Lys His His Arg Glu Glu Val 770 775 780 Tyr Met Ala Ala Gly His Ala Leu Arg Lys Lys Val Gln Phe Ala Lys 785 790 795 800 Asp Glu Asp Leu His Asp Ile Leu Asp Tyr Trp Lys Gly Val Ser Ala 805 810 815 Gln Gln Lys Leu 820 32 866 PRT Homo sapiens 32 Met Thr Ile Glu Lys Met Phe Ser Phe Tyr Phe Leu Asp Tyr Phe Ser 1 5 10 15 Leu Phe Arg Ser Ile Gln Leu Phe Ala Asp Cys Lys Lys Met Phe Leu 20 25 30 Trp Leu Phe Leu Ile Leu Ser Ala Leu Ile Ser Ser Thr Asn Ala Asp 35 40 45 Ser Asp Ile Ser Val Glu Ile Cys Asn Val Cys Ser Cys Val Ser Val 50 55 60 Glu Asn Val Leu Tyr Val Asn Cys Glu Lys Val Ser Val Tyr Arg Pro 65 70 75 80 Asn Gln Leu Lys Pro Pro Trp Ser Asn Phe Tyr His Leu Asn Phe Gln 85 90 95 Asn Asn Phe Leu Asn Ile Leu Tyr Pro Asn Thr Phe Leu Asn Phe Ser 100 105 110 His Ala Val Ser Leu His Leu Gly Asn Asn Lys Leu Gln Asn Ile Glu 115 120 125 Gly Gly Ala Phe Leu Gly Leu Ser Ala Leu Lys Gln Leu His Leu Asn 130 135 140 Asn Asn Glu Leu Lys Ile Leu Arg Ala Asp Thr Phe Leu Gly Ile Glu 145 150 155 160 Asn Leu Glu Tyr Leu Gln Ala Asp Tyr Asn Leu Ile Lys Tyr Ile Glu 165 170 175 Arg Gly Ala Phe Asn Lys Leu His Lys Leu Lys Val Leu Ile Leu Asn 180 185 190 Asp Asn Leu Ile Ser Phe Leu Pro Asp Asn Ile Phe Arg Phe Ala Ser 195 200 205 Leu Thr His Leu Asp Ile Arg Gly Asn Arg Ile Gln Lys Leu Pro Tyr 210 215 220 Ile Gly Val Leu Glu His Ile Gly Arg Val Val Glu Leu Gln Leu Glu 225 230 235 240 Asp Asn Pro Trp Asn Cys Ser Cys Asp Leu Leu Pro Leu Lys Ala Trp 245 250 255 Leu Glu Asn Met Pro Tyr Asn Ile Tyr Ile Gly Glu Ala Ile Cys Glu 260 265 270 Thr Pro Ser Asp Leu Tyr Gly Arg Leu Leu Lys Glu Thr Asn Lys Gln 275 280 285 Glu Leu Cys Pro Met Gly Thr Gly Ser Asp Phe Asp Val Arg Ile Leu 290 295 300 Pro Pro Ser Gln Leu Glu Asn Gly Tyr Thr Thr Pro Asn Gly His Thr 305 310 315 320 Thr Gln Thr Ser Leu His Arg Leu Val Thr Lys Pro Pro Lys Thr Thr 325 330 335 Asn Pro Ser Lys Ile Ser Gly Ile Val Ala Gly Lys Ala Leu Ser Asn 340 345 350 Arg Asn Leu Ser Gln Ile Val Ser Tyr Gln Thr Arg Val Pro Pro Leu 355 360 365 Thr Pro Cys Pro Ala Pro Cys Phe Cys Lys Thr His Pro Ser Asp Leu 370 375 380 Gly Leu Ser Val Asn Cys Gln Glu Lys Asn Ile Gln Ser Met Ser Glu 385 390 395 400 Leu Ile Pro Lys Pro Leu Asn Ala Lys Lys Leu His Val Asn Gly Asn 405 410 415 Ser Ile Lys Asp Val Asp Val Ser Asp Phe Thr Asp Phe Glu Gly Leu 420 425 430 Asp Leu Leu His Leu Gly Ser Asn Gln Ile Thr Val Ile Lys Gly Asp 435 440 445 Val Phe His Asn Leu Thr Asn Leu Arg Arg Leu Tyr Leu Asn Gly Asn 450 455 460 Gln Ile Glu Arg Leu Tyr Pro Glu Ile Phe Ser Gly Leu His Asn Leu 465 470 475 480 Gln Tyr Leu Tyr Leu Glu Tyr Asn Leu Ile Lys Glu Ile Ser Ala Gly 485 490 495 Thr Phe Asp Ser Met Pro Asn Leu Gln Leu Leu Tyr Leu Asn Asn Asn 500 505 510 Leu Leu Lys Ser Leu Pro Val Tyr Ile Phe Ser Gly Ala Pro Leu Ala 515 520 525 Arg Leu Asn Leu Arg Asn Asn Lys Phe Met Tyr Leu Pro Val Ser Gly 530 535 540 Val Leu Asp Gln Leu Gln Ser Leu Thr Gln Ile Asp Leu Glu Gly Asn 545 550 555 560 Pro Trp Asp Cys Thr Cys Asp Leu Val Ala Leu Lys Leu Trp Val Glu 565 570 575 Lys Leu Ser Asp Gly Ile Val Val Lys Glu Leu Lys Cys Glu Thr Pro 580 585 590 Val Gln Phe Ala Asn Ile Glu Leu Lys Ser Leu Lys Asn Glu Ile Leu 595 600 605 Cys Pro Lys Leu Leu Asn Lys Pro Ser Ala Pro Phe Thr Ser Pro Ala 610 615 620 Pro Ala Ile Thr Phe Thr Thr Pro Leu Gly Pro Ile Arg Ser Pro Pro 625 630 635 640 Gly Gly Pro Val Pro Leu Ser Ile Leu Ile Leu Ser Ile Leu Val Val 645 650 655 Leu Ile Leu Thr Val Phe Val Ala Phe Cys Leu Leu Val Phe Val Leu 660 665 670 Arg Arg Asn Lys Lys Pro Thr Val Lys His Glu Gly Leu Gly Asn Pro 675 680 685 Asp Cys Gly Ser Met Gln Leu Gln Leu Arg Lys His Asp His Lys Thr 690 695 700 Asn Lys Lys Asp Gly Leu Ser Thr Glu Ala Phe Ile Pro Gln Thr Ile 705 710 715 720 Glu Gln Met Ser Lys Ser His Thr Cys Gly Leu Lys Glu Ser Glu Thr 725 730 735 Gly Phe Met Phe Ser Asp Pro Pro Gly Gln Lys Val Val Met Arg Asn 740 745 750 Val Ala Asp Lys Glu Lys Asp Leu Leu His Val Asp Thr Arg Lys Arg 755 760 765 Leu Ser Thr Ile Asp Glu Leu Asp Glu Leu Phe Pro Ser Arg Asp Ser 770 775 780 Asn Val Phe Ile Gln Asn Phe Leu Glu Ser Lys Lys Glu Tyr Asn Ser 785 790 795 800 Ile Gly Val Ser Gly Phe Glu Ile Arg Tyr Pro Glu Lys Gln Pro Asp 805 810 815 Lys Lys Ser Lys Lys Ser Leu Ile Gly Gly Asn His Ser Lys Ile Val 820 825 830 Val Glu Gln Arg Lys Ser Glu Tyr Phe Glu Leu Lys Ala Lys Leu Gln 835 840 845 Ser Ser Pro Asp Tyr Leu Gln Val Leu Glu Glu Gln Thr Ala Leu Asn 850 855 860 Lys Ile 865 33 533 PRT Homo sapiens 33 Met Ala Pro Gly Pro Phe Ser Ser Ala Leu Leu Ser Pro Pro Pro Ala 1 5 10 15 Ala Leu Pro Phe Leu Leu Leu Leu Trp Ala Gly Ala Ser Arg Gly Gln 20 25 30 Pro Cys Pro Gly Arg Cys Ile Cys Gln Asn Val Ala Pro Thr Leu Thr 35 40 45 Met Leu Cys Ala Lys Thr Gly Leu Leu Phe Val Pro Pro Ala Ile Asp 50 55 60 Arg Arg Val Val Glu Leu Arg Leu Thr Asp Asn Phe Ile Ala Ala Val 65 70 75 80 Arg Arg Arg Asp Phe Ala Asn Met Thr Ser Leu Val His Leu Thr Leu 85 90 95 Ser Arg Asn Thr Ile Gly Gln Val Ala Ala Gly Ala Phe Ala Asp Leu 100 105 110 Arg Ala Leu Arg Ala Leu His Leu Asp Ser Asn Arg Leu Ala Glu Val 115 120 125 Arg Gly Asp Gln Leu Arg Gly Leu Gly Asn Leu Arg His Leu Ile Leu 130 135 140 Gly Asn Asn Gln Ile Arg Arg Val Glu Ser Ala Ala Phe Asp Ala Phe 145 150 155 160 Leu Ser Thr Val Glu Asp Leu Asp Leu Ser Tyr Asn Asn Leu Glu Ala 165 170 175 Leu Pro Trp Glu Ala Val Gly Gln Met Val Asn Leu Asn Thr Leu Thr 180 185 190 Leu Asp His Asn Leu Ile Asp His Ile Ala Glu Gly Thr Phe Val Gln 195 200 205 Leu His Lys Leu Val Arg Leu Asp Met Thr Ser Asn Arg Leu His Lys 210 215 220 Leu Pro Pro Asp Gly Leu Phe Leu Arg Ser Gln Gly Thr Gly Pro Lys 225 230 235 240 Pro Pro Thr Pro Leu Thr Val Ser Phe Gly Gly Asn Pro Leu His Cys 245 250 255 Asn Cys Glu Leu Leu Trp Leu Arg Arg Leu Thr Arg Glu Asp Asp Leu 260 265 270 Glu Thr Cys Ala Thr Pro Glu His Leu Thr Asp Arg Tyr Phe Trp Ser 275 280 285 Ile Pro Glu Glu Glu Phe Leu Cys Glu Pro Pro Leu Ile Thr Arg Gln 290 295 300 Ala Gly Gly Arg Ala Leu Val Val Glu Gly Gln Ala Val Ser Leu Arg 305 310 315 320 Cys Arg Ala Val Gly Asp Pro Glu Pro Val Val His Trp Val Ala Pro 325 330 335 Asp Gly Arg Leu Leu Gly Asn Ser Ser Arg Thr Arg Val Arg Gly Asp 340 345 350 Gly Thr Leu Asp Val Thr Ile Thr Thr Leu Arg Asp Ser Gly Thr Phe 355 360 365 Thr Cys Ile Ala Ser Asn Ala Ala Gly Glu Ala Thr Ala Pro Val Glu 370 375 380 Val Cys Val Val Pro Leu Pro Leu Met Ala Pro Pro Pro Ala Ala Pro 385 390 395 400 Pro Pro Leu Thr Glu Pro Gly Ser Ser Asp Ile Ala Thr Pro Gly Arg 405 410 415 Pro Gly Ala Asn Asp Ser Ala Ala Glu Arg Arg Leu Val Ala Ala Glu 420 425 430 Leu Thr Ser Asn Ser Val Leu Ile Arg Trp Pro Ala Gln Arg Pro Val 435 440 445 Pro Gly Ile Arg Met Tyr Gln Val Gln Tyr Asn Ser Ser Val Asp Asp 450 455 460 Ser Leu Val Tyr Ser Ser Ala Ser Leu Met His Ile Val Glu His Gln 465 470 475 480 Leu Asn Ala Ser Val Ile Cys Leu Ala Ser Pro Gly Asp Ala Ser Gly 485 490 495 Ala Gly Ala Val Ser Leu Pro Val Glu Ser Leu Ser Ser Trp Leu Ser 500 505 510 Asp Leu His Arg Glu Thr Cys Leu Leu Ala Ser Ile Ser Ala Phe Pro 515 520 525 Val Phe Ser Trp Pro 530 34 771 PRT Homo sapiens 34 Met Ala Pro Gly Pro Phe Ser Ser Ala Leu Leu Ser Pro Pro Pro Ala 1 5 10 15 Ala Leu Pro Phe Leu Leu Leu Leu Trp Ala Gly Ala Ser Arg Gly Gln 20 25 30 Pro Cys Pro Gly Arg Cys Ile Cys Gln Asn Val Ala Pro Thr Leu Thr 35 40 45 Met Leu Cys Ala Lys Thr Gly Leu Leu Phe Val Pro Pro Ala Ile Asp 50 55 60 Arg Arg Val Val Glu Leu Arg Leu Thr Asp Asn Phe Ile Ala Ala Val 65 70 75 80 Arg Arg Arg Asp Phe Ala Asn Met Thr Ser Leu Val His Leu Thr Leu 85 90 95 Ser Arg Asn Thr Ile Gly Gln Val Ala Ala Gly Ala Phe Ala Asp Leu 100 105 110 Arg Ala Leu Arg Ala Leu His Leu Asp Ser Asn Arg Leu Ala Glu Val 115 120 125 Arg Gly Asp Gln Leu Arg Gly Leu Gly Asn Leu Arg His Leu Ile Leu 130 135 140 Gly Asn Asn Gln Ile Arg Arg Val Glu Ser Ala Ala Phe Asp Ala Phe 145 150 155 160 Leu Ser Thr Val Glu Asp Leu Asp Leu Ser Tyr Asn Asn Leu Glu Ala 165 170 175 Leu Pro Trp Glu Ala Val Gly Gln Met Val Asn Leu Asn Thr Leu Thr 180 185 190 Leu Asp His Asn Leu Ile Asp His Ile Ala Glu Gly Thr Phe Val Gln 195 200 205 Leu His Lys Leu Val Arg Leu Asp Met Thr Ser Asn Arg Leu His Lys 210 215 220 Leu Pro Pro Asp Gly Leu Phe Leu Arg Ser Gln Gly Thr Gly Pro Lys 225 230 235 240 Pro Pro Thr Pro Leu Thr Val Ser Phe Gly Gly Asn Pro Leu His Cys 245 250 255 Asn Cys Glu Leu Leu Trp Leu Arg Arg Leu Thr Arg Glu Asp Asp Leu 260 265 270 Glu Thr Cys Ala Thr Pro Glu His Leu Thr Asp Arg Tyr Phe Trp Ser 275 280 285 Ile Pro Glu Glu Glu Phe Leu Cys Glu Pro Pro Leu Ile Thr Arg Gln 290 295 300 Ala Gly Gly Arg Ala Leu Val Val Glu Gly Gln Ala Val Ser Leu Arg 305 310 315 320 Cys Arg Ala Val Gly Asp Pro Glu Pro Val Val His Trp Val Ala Pro 325 330 335 Asp Gly Arg Leu Leu Gly Asn Ser Ser Arg Thr Arg Val Arg Gly Asp 340 345 350 Gly Thr Leu Asp Val Thr Ile Thr Thr Leu Arg Asp Ser Gly Thr Phe 355 360 365 Thr Cys Ile Ala Ser Asn Ala Ala Gly Glu Ala Thr Ala Pro Val Glu 370 375 380 Val Cys Val Val Pro Leu Pro Leu Met Ala Pro Pro Pro Ala Ala Pro 385 390 395 400 Pro Pro Leu Thr Glu Pro Gly Ser Ser Asp Ile Ala Thr Pro Gly Arg 405 410 415 Pro Gly Ala Asn Asp Ser Ala Ala Glu Arg Arg Leu Val Ala Ala Glu 420 425 430 Leu Thr Ser Asn Ser Val Leu Ile Arg Trp Pro Ala Gln Arg Pro Val 435 440 445 Pro Gly Ile Arg Met Tyr Gln Val Gln Tyr Asn Ser Ser Val Asp Asp 450 455 460 Ser Leu Val Tyr Arg Met Ile Pro Ser Thr Ser Gln Thr Phe Leu Val 465 470 475 480 Asn Asp Leu Ala Ala Gly Arg Ala Tyr Asp Leu Cys Val Leu Ala Val 485 490 495 Tyr Asp Asp Gly Ala Thr Ala Leu Pro Ala Thr Arg Val Val Gly Cys 500 505 510 Val Gln Phe Thr Thr Ala Gly Asp Pro Ala Pro Cys Arg Pro Leu Arg 515 520 525 Ala His Phe Leu Gly Gly Thr Met Ile Ile Ala Ile Gly Gly Val Ile 530 535 540 Val Ala Ser Val Leu Val Phe Ile Val Leu Leu Met Ile Arg Tyr Lys 545 550 555 560 Val Tyr Gly Asp Gly Asp Ser Arg Arg Val Lys Gly Ser Arg Ser Leu 565 570 575 Pro Arg Val Ser His Val Cys Ser Gln Thr Asn Gly Ala Gly Thr Gly 580 585 590 Ala Ala Gln Ala Pro Ala Leu Pro Ala Gln Asp His Tyr Glu Ala Leu 595 600 605 Arg Glu Val Glu Ser Gln Ala Ala Pro Ala Val Ala Val Glu Ala Lys 610 615 620 Ala Met Glu Ala Glu Thr Ala Ser Ala Glu Pro Glu Val Val Leu Gly 625 630 635 640 Arg Ser Leu Gly Gly Ser Ala Thr Ser Leu Cys Leu Leu Pro Ser Glu 645 650 655 Glu Thr Ser Gly Glu Glu Ser Arg Ala Ala Val Gly Pro Arg Arg Ser 660 665 670 Arg Ser Gly Ala Leu Glu Pro Pro Thr Ser Ala Pro Pro Thr Leu Ala 675 680 685 Leu Val Pro Gly Gly Ala Ala Ala Arg Pro Arg Pro Gln Gln Arg Tyr 690 695 700 Ser Phe Asp Gly Asp Tyr Gly Ala Leu Phe Gln Ser His Ser Tyr Pro 705 710 715 720 Arg Arg Ala Arg Arg Thr Lys Arg His Arg Ser Thr Pro His Leu Asp 725 730 735 Gly Ala Gly Gly Gly Ala Ala Gly Glu Asp Gly Asp Leu Gly Leu Gly 740 745 750 Ser Ala Arg Ala Cys Leu Ala Phe Thr Ser Thr Glu Trp Met Leu Glu 755 760 765 Ser Thr Val 770 35 399 PRT Homo sapiens 35 Met Trp Gln Leu Leu Ala Ala Ala Cys Trp Met Leu Leu Leu Gly Ser 1 5 10 15 Met Tyr Gly Tyr Asp Lys Lys Gly Asn Asn Ala Asn Pro Glu Ala Asn 20 25 30 Met Asn Ile Ser Gln Ile Ile Ser Tyr Trp Gly Tyr Pro Tyr Glu Glu 35 40 45 Tyr Asp Val Thr Thr Lys Asp Gly Tyr Ile Leu Gly Ile Tyr Arg Ile 50 55 60 Pro His Gly Arg Gly Cys Pro Gly Arg Thr Ala Pro Lys Pro Ala Val 65 70 75 80 Tyr Leu Gln His Gly Leu Ile Ala Ser Ala Ser Asn Trp Ile Cys Asn 85 90 95 Leu Pro Asn Asn Ser Leu Ala Phe Leu Leu Ala Asp Ser Gly Tyr Asp 100 105 110 Val Trp Leu Gly Asn Ser Arg Gly Asn Thr Trp Ser Arg Lys His Leu 115 120 125 Lys Leu Ser Pro Lys Ser Pro Glu Tyr Trp Ala Phe Ser Leu Asp Glu 130 135 140 Met Ala Lys Tyr Asp Leu Pro Ala Thr Ile Asn Phe Ile Ile Glu Lys 145 150 155 160 Thr Gly Gln Lys Arg Leu Tyr Tyr Val Gly His Ser Gln Gly Thr Thr 165 170 175 Ile Ala Phe Ile Ala Phe Ser Thr Asn Pro Glu Leu Ala Lys Lys Ile 180 185 190 Lys Ile Phe Phe Ala Leu Ala Pro Val Val Thr Val Lys Tyr Thr Gln 195 200 205 Ser Pro Met Lys Lys Leu Thr Thr Leu Ser Arg Arg Val Val Lys Val 210 215 220 Leu Phe Gly Asp Lys Met Phe His Pro His Thr Leu Phe Asp Gln Phe 225 230 235 240 Ile Ala Thr Lys Val Cys Asn Arg Lys Leu Phe Arg Arg Ile Cys Ser 245 250 255 Asn Phe Leu Phe Thr Leu Ser Gly Phe Asp Pro Gln Asn Leu Asn Met 260 265 270 Ser Arg Leu Asp Val Tyr Leu Ser His Asn Pro Ala Gly Thr Ser Val 275 280 285 Gln Asn Met Leu His Trp Ala Gln Ala Val Asn Ser Gly Gln Leu Gln 290 295 300 Ala Phe Asp Trp Gly Asn Ser Asp Gln Asn Met Met His Phe His Gln 305 310 315 320 Leu Thr Pro Pro Leu Tyr Asn Ile Thr Lys Ile Glu Val Pro Thr Ala 325 330 335 Ile Trp Asn Gly Gly Gln Asp Ile Val Ala Asp Pro Lys Asp Val Glu 340 345 350 Asn Leu Leu Pro Gln Ile Ala Asn Leu Ile Tyr Tyr Lys Leu Ile Pro 355 360 365 His Tyr Asn His Val Asp Phe Tyr Leu Gly Glu Asp Ala Pro Gln Glu 370 375 380 Ile Tyr Gln Asp Leu Ile Ile Leu Met Glu Glu Tyr Leu Gln Asn 385 390 395 36 255 PRT Homo sapiens 36 Ile Val Gly Gly Ser Asn Ala Gln Pro Gly Thr Trp Pro Trp Gln Val 1 5 10 15 Ser Leu His His Gly Gly Gly His Ile Cys Gly Gly Ser Leu Ile Ala 20 25 30 Pro Ser Trp Val Leu Ser Ala Ala His Cys Phe Met Thr Gly Arg Gln 35 40 45 Tyr Arg Cys Pro Glu Thr Arg Arg Thr Arg Ser Ala Leu Pro Thr Arg 50 55 60 Lys Arg Arg Arg Ala Tyr Asn His Tyr Ser Gln Gly Ser Asp Leu Ala 65 70 75 80 Leu Leu Gln Leu Ala His Pro Thr Thr His Thr Pro Leu Cys Leu Pro 85 90 95 Gln Pro Ala His Arg Phe Pro Phe Gly Ala Ser Cys Trp Ala Thr Gly 100 105 110 Trp Asp Gln Asp Thr Ser Asp Ala Pro Ser Leu Ser Pro Ala Pro Gly 115 120 125 Thr Leu Arg Asn Leu Arg Leu Arg Leu Ile Ser Arg Pro Thr Cys Asn 130 135 140 Cys Ile Tyr Asn Gln Leu His Gln Arg His Leu Ser Asn Pro Ala Arg 145 150 155 160 Pro Gly Met Leu Cys Gly Gly Pro Gln Pro Gly Val Gln Gly Pro Cys 165 170 175 Gln Gly Leu Phe Gly Ala Pro Leu Val His Glu Val Arg Gly Thr Trp 180 185 190 Phe Leu Ala Gly Leu His Ser Phe Gly Asp Ala Cys Gln Gly Pro Ala 195 200 205 Arg Pro Ala Val Phe Thr Ala Leu Pro Ala Met Arg Thr Gly Ser Ala 210 215 220 Val Trp Thr Arg Gln Val Tyr Phe Ala Glu Glu Pro Glu Pro Glu Ala 225 230 235 240 Glu Pro Gly Ser Cys Leu Ala Asn Ile Arg Pro Phe Ser Leu Gln 245 250 255 37 301 PRT Homo sapiens 37 Met Glu Thr Ala Gly Ser Asp Trp Val Ala Gly Gly Pro Leu Thr Gln 1 5 10 15 Ala Ser His Pro Ser Glu Cys Gly Lys Ala Pro Arg Pro Gly Ala Trp 20 25 30 Pro Trp Glu Ala Gln Val Met Val Pro Gly Ser Arg Pro Cys His Gly 35 40 45 Ala Leu Val Ser Glu Ser Trp Val Leu Ala Pro Ala Ser Cys Phe Leu 50 55 60 Glu Gln Val Thr His Thr Leu Cys Cys Cys Arg Met Thr Arg Val Gly 65 70 75 80 Ala Phe Cys Ala Arg Arg Arg Gly Pro Gly Phe Trp Leu Glu Ser Glu 85 90 95 Thr Phe Pro Val Ala Val Tyr Leu Pro Arg Ala Tyr Asn His Tyr Ser 100 105 110 Gln Gly Ser Asp Leu Ala Leu Leu Gln Leu Ala His Pro Thr Thr His 115 120 125 Thr Pro Leu Cys Leu Pro Gln Pro Ala His Arg Phe Pro Phe Gly Ala 130 135 140 Ser Cys Trp Ala Thr Gly Trp Asp Gln Asp Thr Ser Asp Ala Pro Gly 145 150 155 160 Thr Leu Arg Asn Leu Arg Leu Arg Leu Ile Ser Arg Pro Thr Cys Asn 165 170 175 Cys Ile Tyr Asn Gln Leu His Gln Arg His Leu Ser Asn Pro Ala Arg 180 185 190 Pro Gly Met Leu Cys Gly Gly Pro Gln Pro Gly Val Gln Gly Pro Cys 195 200 205 Gln Gly Leu Phe Gly Ala Pro Leu Val His Glu Val Arg Gly Thr Trp 210 215 220 Phe Leu Ala Gly Leu His Ser Phe Gly Asp Ala Cys Gln Gly Pro Ala 225 230 235 240 Arg Pro Ala Val Phe Thr Ala Leu Pro Ala Met Arg Thr Gly Ser Ala 245 250 255 Val Trp Thr Arg Gln Val Tyr Phe Ala Glu Glu Pro Glu Pro Glu Ala 260 265 270 Glu Pro Gly Ser Cys Leu Ala Asn Ile Ser Met Trp Pro Arg Gly Leu 275 280 285 Leu Pro Asn Pro Ala Ser Pro Gly Pro Phe Ser Leu Gln 290 295 300 38 383 PRT Homo sapiens 38 Met Pro Ser Gly Cys Arg Cys Leu His Leu Val Cys Leu Leu Cys Ile 1 5 10 15 Leu Gly Ala Pro Gly Gln Pro Val Arg Ala Asp Asp Cys Ser Ser His 20 25 30 Cys Asp Leu Ala His Gly Cys Cys Ala Pro Asp Gly Ser Cys Arg Cys 35 40 45 Asp Pro Gly Trp Glu Gly Leu His Cys Glu Arg Cys Val Arg Met Pro 50 55 60 Gly Cys Gln His Gly Thr Cys His Gln Pro Trp Gln Cys Ile Cys His 65 70 75 80 Ser Gly Trp Ala Gly Lys Phe Cys Asp Lys Asp Glu His Ile Cys Thr 85 90 95 Thr Gln Ser Pro Cys Gln Asn Gly Gly Gln Cys Met Tyr Asp Gly Gly 100 105 110 Gly Glu Tyr His Cys Val Cys Leu Pro Gly Phe His Gly Arg Asp Cys 115 120 125 Glu Arg Lys Ala Gly Pro Cys Glu Gln Ala Gly Ser Pro Cys Arg Asn 130 135 140 Gly Gly Gln Cys Gln Asp Asp Gln Gly Phe Ala Leu Asn Phe Thr Cys 145 150 155 160 Arg Cys Leu Val Gly Phe Val Gly Ala Arg Cys Glu Val Asn Val Asp 165 170 175 Asp Cys Leu Met Arg Pro Cys Ala Asn Gly Ala Thr Cys Leu Asp Gly 180 185 190 Ile Asn Arg Phe Ser Cys Leu Cys Pro Glu Gly Phe Ala Gly Arg Phe 195 200 205 Cys Thr Ile Asn Leu Asp Asp Cys Ala Ser Arg Pro Cys Gln Arg Gly 210 215 220 Ala Arg Cys Arg Asp Arg Val His Asp Phe Asp Cys Leu Cys Pro Ser 225 230 235 240 Gly Tyr Gly Gly Lys Thr Cys Glu Leu Val Leu Pro Val Pro Asp Pro 245 250 255 Pro Thr Thr Val Asp Thr Pro Leu Gly Pro Thr Ser Ala Val Val Val 260 265 270 Pro Ala Thr Gly Pro Ala Pro His Ser Ala Gly Ala Gly Leu Leu Arg 275 280 285 Ile Ser Val Lys Glu Val Val Arg Arg Gln Glu Ala Gly Leu Gly Glu 290 295 300 Pro Ser Leu Val Ala Leu Val Val Phe Gly Ala Leu Thr Ala Ala Leu 305 310 315 320 Val Leu Ala Thr Val Leu Leu Thr Leu Arg Ala Trp Arg Arg Gly Val 325 330 335 Cys Pro Pro Gly Pro Cys Cys Tyr Pro Ala Pro His Tyr Ala Pro Ala 340 345 350 Cys Gln Asp Gln Glu Cys Gln Val Ser Met Leu Pro Ala Gly Leu Pro 355 360 365 Leu Pro Arg Asp Leu Pro Pro Glu Pro Gly Lys Thr Thr Ala Leu 370 375 380 39 417 PRT Homo sapiens 39 Met Ala Ser Tyr Leu Tyr Gly Val Leu Phe Ala Val Gly Leu Cys Ala 1 5 10 15 Pro Ile Tyr Cys Val Ser Pro Ala Asn Ala Pro Ser Ala Tyr Pro Arg 20 25 30 Pro Ser Ser Thr Lys Ser Thr Pro Ala Ser Gln Val Tyr Ser Leu Asn 35 40 45 Thr Asp Phe Ala Phe Arg Leu Tyr Arg Arg Leu Val Leu Glu Thr Pro 50 55 60 Ser Gln Asn Ile Phe Phe Ser Pro Val Ser Val Ser Thr Ser Leu Ala 65 70 75 80 Met Leu Ser Leu Gly Ala His Ser Val Thr Lys Thr Gln Ile Leu Gln 85 90 95 Gly Leu Gly Phe Asn Leu Thr His Thr Pro Glu Ser Ala Ile His Gln 100 105 110 Gly Phe Gln His Leu Val His Ser Leu Thr Val Pro Ser Lys Asp Leu 115 120 125 Thr Leu Lys Met Gly Ser Ala Leu Phe Val Lys Lys Glu Leu Gln Leu 130 135 140 Gln Ala Asn Phe Leu Gly Asn Val Lys Arg Leu Tyr Glu Ala Glu Val 145 150 155 160 Phe Ser Thr Asp Phe Ser Asn Pro Ser Ile Ala Gln Ala Arg Ile Asn 165 170 175 Ser His Val Lys Lys Lys Thr Gln Gly Lys Val Val Asp Ile Ile Gln 180 185 190 Gly Leu Asp Leu Leu Thr Ala Met Val Leu Val Asn His Ile Phe Phe 195 200 205 Lys Ala Lys Trp Glu Lys Pro Phe His Pro Glu Tyr Thr Arg Lys Asn 210 215 220 Phe Pro Phe Leu Val Gly Glu Gln Val Thr Val His Val Pro Met Met 225 230 235 240 His Gln Lys Glu Gln Phe Ala Phe Gly Val Asp Thr Glu Leu Asn Cys 245 250 255 Phe Val Leu Gln Met Asp Tyr Lys Gly Asp Ala Val Ala Phe Phe Val 260 265 270 Leu Pro Ser Lys Gly Lys Met Arg Gln Leu Glu Gln Ala Leu Ser Ala 275 280 285 Arg Thr Leu Arg Lys Trp Ser His Ser Leu Gln Lys Arg Trp Ile Glu 290 295 300 Val Phe Ile Pro Arg Phe Ser Ile Ser Ala Ser Tyr Asn Leu Glu Thr 305 310 315 320 Ile Leu Pro Lys Met Gly Ile Gln Asn Val Phe Asp Lys Asn Ala Asp 325 330 335 Phe Ser Gly Ile Ala Lys Arg Asp Ser Leu Gln Val Ser Lys Ala Thr 340 345 350 His Lys Ala Val Leu Asp Val Ser Glu Glu Gly Thr Glu Ala Thr Ala 355 360 365 Ala Thr Thr Thr Lys Phe Ile Val Arg Ser Lys Asp Gly Pro Ser Tyr 370 375 380 Phe Thr Val Ser Phe Asn Arg Thr Phe Leu Met Met Ile Thr Asn Lys 385 390 395 400 Ala Thr Asp Gly Ile Leu Phe Leu Gly Lys Val Glu Asn Pro Thr Lys 405 410 415 Ser 40 243 PRT Homo sapiens 40 Met Gly Ser Ser Ser Phe Leu Val Leu Met Val Ser Leu Val Leu Val 1 5 10 15 Thr Leu Val Ala Val Glu Gly Val Lys Glu Gly Ile Glu Lys Ala Gly 20 25 30 Val Cys Pro Ala Asp Asn Val Arg Cys Phe Lys Ser Asp Pro Pro Gln 35 40 45 Cys His Thr Asp Gln Asp Cys Leu Gly Glu Arg Lys Cys Cys Tyr Leu 50 55 60 His Cys Gly Phe Lys Cys Val Ile Pro Val Lys Glu Leu Glu Glu Gly 65 70 75 80 Gln Arg Leu Leu His Asn Arg Glu Leu Pro Pro Ala Ala Ile Leu Gly 85 90 95 Asp Ser Leu Thr Glu Lys Ser Gly Gly Cys Pro Pro Asp Asp Gly Pro 100 105 110 Cys Leu Leu Ser Val Pro Asp Gln Cys Val Glu Asp Ser Gln Cys Pro 115 120 125 Leu Thr Arg Lys Cys Cys Tyr Arg Ala Cys Phe Arg Gln Cys Val Pro 130 135 140 Arg Val Ser Gly Lys Cys Leu Pro Ser Thr Leu Leu Thr Ile Gln Ala 145 150 155 160 Pro Ser Phe Arg Ala Ser Gly Gln Gly Arg Ser Ser Pro Ser Ser Leu 165 170 175 Cys Cys Ser Glu Ala Gly Gln Leu Pro Arg Gly Pro Thr Ala Leu Pro 180 185 190 Gln Pro His Glu Pro Pro Val Ser Gln Gly Leu Arg Leu Leu Gly Gln 195 200 205 Lys Ala Met Leu Pro Gln Arg Leu Arg Ala Gly Leu Pro Gly Ser Cys 210 215 220 Gln Arg Tyr Gly Ser Trp Val Pro Arg Ala Gly Ala Ser Pro Leu Arg 225 230 235 240 Ala Gln Leu 41 185 PRT Homo sapiens 41 Met Gly Ser Ser Ser Phe Leu Val Leu Met Val Ser Leu Val Leu Val 1 5 10 15 Thr Leu Val Ala Val Glu Gly Val Lys Glu Gly Ile Glu Lys Ala Gly 20 25 30 Val Cys Pro Ala Asp Asn Val Arg Cys Phe Lys Ser Asp Pro Pro Gln 35 40 45 Cys His Thr Asp Gln Asp Cys Leu Gly Glu Arg Lys Cys Cys Tyr Leu 50 55 60 His Cys Gly Phe Lys Cys Val Ile Pro Val Lys Glu Leu Glu Glu Val 65 70 75 80 Pro Cys Val Ala Val Lys Leu Gly Ser Cys Pro Glu Asp Gln Leu Arg 85 90 95 Cys Leu Ser Pro Met Asn His Leu Cys His Lys Asp Ser Asp Cys Ser 100 105 110 Gly Lys Lys Arg Cys Cys His Ser Ala Cys Gly Arg Asp Cys Arg Asp 115 120 125 Pro Ala Arg Gly Thr Ala Pro Gly Cys Pro Gly Gln Val Pro Pro Leu 130 135 140 Ser Glu Pro Ser Ser Asn Thr Phe Phe Ile Ala Thr Ser Leu Thr Gly 145 150 155 160 Cys Leu Pro Arg Ser Gln Asp Leu Pro Trp Pro Gly Leu Gly Asn Trp 165 170 175 Ile Gly Val Gly Gly Val Leu Leu Gly 180 185 42 198 PRT Homo sapiens 42 Met Asn Ser Gly Arg Glu Pro Arg Thr Pro Arg Thr Leu Leu Ser Ile 1 5 10 15 Ala Asp Ile Leu Ala Pro Arg Met Val Pro Arg Ala Pro Ser Ala Pro 20 25 30 Gln Leu Pro Glu Ser Gly Pro Gly Pro Thr Ser Pro Leu Cys Ala Leu 35 40 45 Glu Glu Leu Thr Ser Lys Thr Phe Arg Gly Leu Asp Ala Arg Ala Leu 50 55 60 Gln Pro Ser Glu Gly Arg Ala Gly Pro Asp Ala Leu Gly Pro Gly Pro 65 70 75 80 Phe Gly Arg Lys Arg Arg Lys Ser Arg Thr Ala Phe Thr Ala Gln Gln 85 90 95 Val Leu Glu Leu Glu Arg Arg Phe Val Phe Gln Lys Tyr Leu Ala Pro 100 105 110 Ser Glu Arg Asp Gly Leu Ala Thr Arg Leu Gly Leu Ala Asn Ala Gln 115 120 125 Val Val Thr Trp Phe Gln Asn Arg Arg Ala Lys Leu Lys Arg Asp Val 130 135 140 Glu Glu Met Arg Ala Asp Val Ala Ser Leu Arg Ala Leu Ser Pro Glu 145 150 155 160 Val Leu Cys Ser Leu Ala Leu Pro Glu Gly Ala Pro Asp Pro Gly Leu 165 170 175 Cys Leu Gly Pro Ala Gly Pro Asp Ser Arg Pro His Leu Ser Asp Glu 180 185 190 Glu Ile Gln Val Asp Asp 195 43 330 PRT Homo sapiens 43 Met Val Trp Lys Arg Glu Asn Phe Tyr Lys Glu Val Lys Arg Gly Arg 1 5 10 15 Ala Leu Phe Leu Lys Arg Leu Cys Ile Phe Asn Ile Asp Thr Asp Asn 20 25 30 Thr Phe Gln Arg Ile Ile Glu Lys Pro Ser Trp Leu Gly Phe Leu Gly 35 40 45 Pro Met Ile Lys Ala Glu Thr Gly Asp Phe Ile Tyr Val His Val Lys 50 55 60 Asn Asn Ala Ser Arg Ala Tyr Ser Tyr His Pro His Gly Leu Thr Tyr 65 70 75 80 Ser Lys Glu Asn Glu Gly Ala Ile Tyr Pro Asp Asn Thr Thr Gly Leu 85 90 95 Gln Lys Glu Asp Glu Tyr Leu Glu Pro Gly Lys Gln Tyr Thr Tyr Lys 100 105 110 Trp Tyr Val Glu Glu His Gln Gly Pro Gly Pro Asn Asp Ser Asn Cys 115 120 125 Val Thr Arg Ile Tyr His Ser His Ile Asp Thr Ala Arg Asp Val Ala 130 135 140 Ser Gly Leu Ile Gly Pro Ile Leu Thr Cys Lys Arg Ala Ile Asn Gly 145 150 155 160 Tyr Ile Tyr Gly Asn Leu Pro Asn Leu Thr Met Cys Ala Glu Asp Arg 165 170 175 Val Gln Trp Tyr Phe Val Gly Met Gly Gly Val Ala Asp Ile His Pro 180 185 190 Val Tyr Leu Arg Gly Gln Thr Leu Ile Ser Arg Asn His Arg Lys Asp 195 200 205 Thr Ile Met Leu Phe Pro Ser Ser Leu Glu Asp Ala Phe Met Val Ala 210 215 220 Lys Ala Pro Gly Val Trp Met Leu Gly Cys Gln Ile His Gly Ser Asp 225 230 235 240 Ile Leu Leu Leu Arg Asp Thr Lys Ser Glu Asn Phe Gln Gly Leu Ser 245 250 255 Pro Phe His Met His Phe Leu Thr Asn Glu Glu Thr Tyr Ile Gln Glu 260 265 270 Glu Ser Met Gln Ala Phe Phe Lys Val Ser Asn Cys Gln Lys Pro Ser 275 280 285 Thr Glu Ala Phe Val Thr Gly Thr His Val Ile His Tyr Tyr Ile Ala 290 295 300 Ala Lys Glu Ile Leu Trp Asn Tyr Ala Pro Ser Gly Ile Asp Phe Phe 305 310 315 320 Thr Lys Lys Asn Leu Thr Ala Ala Gly Arg 325 330 44 479 PRT Homo sapiens 44 Met Ala Ile Leu Pro Leu Leu Leu Cys Leu Leu Pro Leu Ala Pro Ala 1 5 10 15 Ser Ser Pro Pro Gln Ser Ala Thr Pro Ser Pro Cys Pro Arg Arg Cys 20 25 30 Arg Cys Gln Thr Gln Ser Leu Pro Leu Ser Val Leu Cys Pro Gly Ala 35 40 45 Gly Leu Leu Phe Val Pro Pro Ser Leu Asp Arg Arg Ala Ala Glu Leu 50 55 60 Arg Leu Ala Asp Asn Phe Ile Ala Ser Val Arg Arg Arg Asp Leu Ala 65 70 75 80 Asn Met Thr Gly Leu Leu His Leu Ser Leu Ser Arg Asn Thr Ile Arg 85 90 95 His Val Ala Ala Gly Ala Phe Ala Asp Leu Arg Ala Leu Arg Ala Leu 100 105 110 His Leu Asp Gly Asn Arg Leu Thr Ser Leu Gly Glu Gly Gln Leu Arg 115 120 125 Gly Leu Val Asn Leu Arg His Leu Ile Leu Ser Asn Asn Gln Leu Ala 130 135 140 Ala Leu Ala Ala Gly Ala Leu Asp Asp Cys Ala Glu Thr Leu Glu Asp 145 150 155 160 Leu Asp Leu Ser Tyr Asn Asn Leu Glu Gln Leu Pro Trp Glu Ala Leu 165 170 175 Gly Arg Leu Gly Asn Val Asn Thr Leu Gly Leu Asp His Asn Leu Leu 180 185 190 Ala Ser Val Pro Ala Gly Ala Phe Ser Arg Leu His Lys Leu Ala Arg 195 200 205 Leu Asp Met Thr Ser Asn Arg Leu Thr Thr Ile Pro Pro Asp Pro Leu 210 215 220 Phe Ser Arg Leu Pro Leu Leu Ala Arg Pro Arg Gly Ser Pro Ala Ser 225 230 235 240 Ala Leu Val Leu Ala Phe Gly Gly Asn Pro Leu His Cys Asn Cys Glu 245 250 255 Leu Val Trp Leu Arg Arg Leu Ala Arg Glu Asp Asp Leu Glu Ala Cys 260 265 270 Ala Ser Pro Pro Ala Leu Gly Gly Arg Tyr Phe Trp Ala Val Gly Glu 275 280 285 Glu Glu Phe Val Cys Glu Pro Pro Val Val Thr His Arg Ser Pro Pro 290 295 300 Leu Ala Val Pro Ala Gly Arg Pro Ala Ala Leu Arg Cys Arg Ala Val 305 310 315 320 Gly Asp Pro Glu Pro Arg Val Arg Trp Val Ser Pro Gln Gly Arg Leu 325 330 335 Leu Gly Asn Ser Ser Arg Ala Arg Ala Phe Pro Asn Gly Thr Leu Glu 340 345 350 Leu Leu Val Thr Glu Pro Gly Asp Gly Gly Ile Phe Thr Cys Ile Ala 355 360 365 Ala Asn Ala Ala Gly Glu Ala Thr Ala Ala Val Glu Leu Thr Val Gly 370 375 380 Pro Pro Pro Pro Pro Gln Leu Ala Asn Ser Thr Ser Cys Asp Pro Pro 385 390 395 400 Arg Asp Gly Asp Pro Asp Ala Leu Thr Pro Pro Ser Ala Ala Ser Ala 405 410 415 Ser Ala Lys Val Ala Asp Thr Gly Pro Pro Thr Asp Arg Gly Val Gln 420 425 430 Val Thr Glu His Gly Ala Thr Ala Ala Leu Val Gln Trp Pro Asp Gln 435 440 445 Arg Pro Ile Pro Gly Ile Arg Met Tyr Gln Ile Gln Tyr Asn Ser Ser 450 455 460 Ala Asp Asp Ile Leu Val Tyr Arg Cys Arg Val Gln Ala Leu Gly 465 470 475 45 628 PRT Homo sapiens 45 Met Ala Ile Leu Pro Leu Leu Leu Cys Leu Leu Pro Leu Ala Pro Ala 1 5 10 15 Ser Ser Pro Pro Gln Ser Ala Thr Pro Ser Pro Cys Pro Arg Arg Cys 20 25 30 Arg Cys Gln Thr Gln Ser Leu Pro Leu Ser Val Leu Cys Pro Gly Ala 35 40 45 Gly Leu Leu Phe Val Pro Pro Ser Leu Asp Arg Arg Ala Ala Glu Leu 50 55 60 Arg Leu Ala Asp Asn Phe Ile Ala Ser Val Arg Arg Arg Asp Leu Ala 65 70 75 80 Asn Met Thr Gly Leu Leu His Leu Ser Leu Ser Arg Asn Thr Ile Arg 85 90 95 His Val Ala Ala Gly Ala Phe Ala Asp Leu Arg Ala Leu Arg Ala Leu 100 105 110 His Leu Asp Gly Asn Arg Leu Thr Ser Leu Gly Glu Gly Gln Leu Arg 115 120 125 Gly Leu Val Asn Leu Arg His Leu Ile Leu Ser Asn Asn Gln Leu Ala 130 135 140 Ala Leu Ala Ala Gly Ala Leu Asp Asp Cys Ala Glu Thr Leu Glu Asp 145 150 155 160 Leu Asp Leu Ser Tyr Asn Asn Leu Glu Gln Leu Pro Trp Glu Ala Leu 165 170 175 Gly Arg Leu Gly Asn Val Asn Thr Leu Gly Leu Asp His Asn Leu Leu 180 185 190 Ala Ser Val Pro Ala Gly Ala Phe Ser Arg Leu His Lys Leu Ala Arg 195 200 205 Leu Asp Met Thr Ser Asn Arg Leu Thr Thr Ile Pro Pro Asp Pro Leu 210 215 220 Phe Ser Arg Leu Pro Leu Leu Ala Arg Pro Arg Gly Ser Pro Ala Ser 225 230 235 240 Ala Leu Val Leu Ala Phe Gly Gly Asn Pro Leu His Cys Asn Cys Glu 245 250 255 Leu Val Trp Leu Arg Arg Leu Ala Arg Glu Asp Asp Leu Glu Ala Cys 260 265 270 Ala Ser Pro Pro Ala Leu Gly Gly Arg Tyr Phe Trp Ala Val Gly Glu 275 280 285 Glu Glu Phe Val Cys Glu Pro Pro Val Val Thr His Arg Ser Pro Pro 290 295 300 Leu Ala Val Pro Ala Gly Arg Pro Ala Ala Leu Arg Cys Arg Ala Val 305 310 315 320 Gly Asp Pro Glu Pro Arg Val Arg Trp Val Ser Pro Gln Gly Arg Leu 325 330 335 Leu Gly Asn Ser Ser Arg Ala Arg Ala Phe Pro Asn Gly Thr Leu Glu 340 345 350 Leu Leu Val Thr Glu Pro Gly Asp Gly Gly Ile Phe Thr Cys Ile Ala 355 360 365 Ala Asn Ala Ala Gly Glu Ala Thr Ala Ala Val Glu Leu Thr Val Gly 370 375 380 Pro Pro Pro Pro Pro Gln Leu Ala Asn Ser Thr Ser Cys Asp Pro Pro 385 390 395 400 Arg Asp Gly Asp Pro Asp Ala Leu Thr Pro Pro Ser Ala Ala Ser Ala 405 410 415 Ser Ala Lys Val Ala Asp Thr Gly Pro Pro Thr Asp Arg Gly Val Gln 420 425 430 Val Thr Glu His Gly Ala Thr Ala Ala Leu Val Gln Trp Pro Asp Gln 435 440 445 Arg Pro Ile Pro Gly Ile Arg Met Tyr Gln Ile Gln Tyr Asn Ser Ser 450 455 460 Ala Asp Asp Ile Leu Val Tyr Arg Met Ile Pro Ala Glu Ser Arg Ser 465 470 475 480 Phe Leu Leu Thr Asp Leu Ala Ser Gly Arg Thr Tyr Asp Leu Cys Val 485 490 495 Leu Ala Val Tyr Glu Asp Ser Ala Thr Gly Leu Thr Ala Thr Arg Pro 500 505 510 Val Gly Cys Ala Arg Phe Ser Thr Glu Pro Ala Leu Arg Pro Cys Gly 515 520 525 Ala Pro His Ala Pro Phe Leu Gly Gly Thr Met Ile Ile Ala Leu Gly 530 535 540 Gly Val Ile Val Ala Ser Val Leu Val Phe Ile Phe Val Leu Leu Met 545 550 555 560 Arg Tyr Lys Val His Gly Gly Gln Pro Pro Gly Lys Ala Lys Ile Pro 565 570 575 Ala Pro Val Ser Ser Val Cys Ser Gln Thr Asn Gly Ala Leu Gly Pro 580 585 590 Thr Pro Thr Pro Ala Pro Pro Ala Pro Glu Pro Ala Ala Leu Arg Ala 595 600 605 His Thr Val Val Gln Leu Asp Cys Glu Pro Trp Gly Pro Gly His Glu 610 615 620 Pro Val Gly Pro 625 46 845 PRT Homo sapiens 46 Met Leu Ser Gly Val Trp Phe Leu Ser Val Leu Thr Val Ala Gly Ile 1 5 10 15 Leu Gln Thr Glu Ser Arg Lys Thr Ala Lys Asp Ile Cys Lys Ile Arg 20 25 30 Cys Leu Cys Glu Glu Lys Glu Asn Val Leu Asn Ile Asn Cys Glu Asn 35 40 45 Lys Gly Phe Thr Thr Val Ser Leu Leu Gln Pro Pro Gln Tyr Arg Ile 50 55 60 Tyr Gln Leu Phe Leu Asn Gly Asn Leu Leu Thr Arg Leu Tyr Pro Asn 65 70 75 80 Glu Phe Val Asn Tyr Ser Asn Ala Val Thr Leu His Leu Gly Asn Asn 85 90 95 Gly Leu Gln Glu Ile Arg Thr Gly Ala Phe Ser Gly Leu Lys Thr Leu 100 105 110 Lys Arg Leu His Leu Asn Asn Asn Lys Leu Glu Ile Leu Arg Glu Asp 115 120 125 Thr Phe Leu Gly Leu Glu Ser Leu Glu Tyr Leu Gln Ala Asp Tyr Asn 130 135 140 Tyr Ile Ser Ala Ile Glu Ala Gly Ala Phe Ser Lys Leu Asn Lys Leu 145 150 155 160 Lys Val Leu Ile Leu Asn Asp Asn Leu Leu Leu Ser Leu Pro Ser Asn 165 170 175 Val Phe Arg Phe Val Leu Leu Thr His Leu Asp Leu Arg Gly Asn Arg 180 185 190 Leu Lys Val Met Pro Phe Ala Gly Val Leu Glu His Ile Gly Gly Ile 195 200 205 Met Glu Ile Gln Leu Glu Glu Asn Pro Trp Asn Cys Thr Cys Asp Leu 210 215 220 Leu Pro Leu Lys Ala Trp Leu Asp Thr Ile Thr Val Phe Val Gly Glu 225 230 235 240 Ile Val Cys Glu Thr Pro Phe Arg Leu His Gly Lys Asp Val Thr Gln 245 250 255 Leu Thr Arg Gln Asp Leu Cys Pro Arg Lys Ser Ala Ser Asp Ser Ser 260 265 270 Gln Arg Gly Ser His Ala Asp Thr His Val Gln Arg Leu Ser Pro Thr 275 280 285 Met Asn Pro Ala Leu Asn Pro Thr Arg Ala Pro Lys Ala Ser Arg Pro 290 295 300 Pro Lys Met Arg Asn Arg Pro Thr Pro Arg Val Thr Val Ser Lys Asp 305 310 315 320 Arg Gln Ser Phe Gly Pro Ile Met Val Tyr Gln Thr Lys Ser Pro Val 325 330 335 Pro Leu Thr Cys Pro Ser Ser Cys Val Cys Thr Ser Gln Ser Ser Asp 340 345 350 Asn Gly Leu Asn Val Asn Cys Gln Glu Arg Lys Phe Thr Asn Ile Ser 355 360 365 Asp Leu Gln Pro Lys Pro Thr Ser Pro Lys Lys Leu Tyr Leu Thr Gly 370 375 380 Asn Tyr Leu Gln Thr Val Tyr Lys Asn Asp Leu Leu Glu Tyr Ser Ser 385 390 395 400 Leu Asp Leu Leu His Leu Gly Asn Asn Arg Ile Ala Val Ile Gln Glu 405 410 415 Gly Ala Phe Thr Asn Leu Thr Ser Leu Arg Arg Leu Tyr Leu Asn Gly 420 425 430 Asn Tyr Leu Glu Val Leu Tyr Pro Ser Met Phe Asp Gly Leu Gln Ser 435 440 445 Leu Gln Tyr Leu Tyr Leu Glu Tyr Asn Val Ile Lys Glu Ile Lys Pro 450 455 460 Leu Thr Phe Asp Ala Leu Ile Asn Leu Gln Leu Leu Phe Leu Asn Asn 465 470 475 480 Asn Leu Leu Arg Ser Leu Pro Asp Asn Ile Phe Gly Gly Thr Ala Leu 485 490 495 Thr Arg Leu Asn Leu Arg Asn Asn His Phe Ser His Leu Pro Val Lys 500 505 510 Gly Val Leu Asp Gln Leu Pro Ala Phe Ile Gln Ile Asp Leu Gln Glu 515 520 525 Asn Pro Trp Asp Cys Thr Cys Asp Ile Met Gly Leu Lys Asp Trp Thr 530 535 540 Glu His Ala Asn Ser Pro Val Ile Ile Asn Glu Val Thr Cys Glu Ser 545 550 555 560 Pro Ala Lys His Ala Gly Glu Ile Leu Lys Phe Leu Gly Arg Glu Ala 565 570 575 Ile Cys Pro Asp Ser Pro Asn Leu Ser Asp Gly Thr Val Leu Ser Met 580 585 590 Asn His Asn Thr Asp Thr Pro Arg Ser Leu Ser Val Ser Pro Ser Ser 595 600 605 Tyr Pro Glu Leu His Thr Glu Val Pro Leu Ser Val Leu Ile Leu Gly 610 615 620 Leu Leu Val Val Phe Ile Leu Ser Val Cys Phe Gly Ala Gly Leu Phe 625 630 635 640 Val Phe Val Leu Lys Arg Arg Lys Gly Val Pro Ser Val Pro Arg Asn 645 650 655 Thr Asn Asn Leu Asp Val Ser Ser Phe Gln Leu Gln Tyr Gly Ser Tyr 660 665 670 Asn Thr Glu Thr His Asp Lys Thr Asp Gly His Val Tyr Asn Tyr Ile 675 680 685 Pro Pro Pro Val Gly Gln Met Cys Gln Asn Pro Ile Tyr Met Gln Lys 690 695 700 Glu Gly Asp Pro Val Ala Tyr Tyr Arg Asn Leu Gln Glu Phe Ser Tyr 705 710 715 720 Ser Asn Leu Glu Glu Lys Lys Glu Glu Pro Ala Thr Pro Ala Tyr Thr 725 730 735 Ile Ser Ala Thr Glu Leu Leu Glu Lys Gln Ala Thr Pro Arg Glu Pro 740 745 750 Glu Leu Leu Tyr Gln Asn Ile Ala Glu Arg Val Lys Glu Leu Pro Ser 755 760 765 Ala Gly Leu Val His Tyr Asn Phe Cys Thr Leu Pro Lys Arg Gln Phe 770 775 780 Ala Pro Ser Tyr Glu Ser Arg Arg Gln Asn Gln Asp Arg Ile Asn Lys 785 790 795 800 Thr Val Leu Tyr Gly Thr Pro Arg Lys Cys Phe Val Gly Gln Ser Lys 805 810 815 Pro Asn His Pro Leu Leu Gln Ala Lys Pro Gln Ser Glu Pro Asp Tyr 820 825 830 Leu Glu Val Leu Glu Lys Gln Thr Ala Ile Ser Gln Leu 835 840 845 47 349 PRT Homo sapiens 47 Met Gly Ile Thr Cys Trp Ile Ala Leu Tyr Ala Val Glu Ala Leu Pro 1 5 10 15 Thr Cys Pro Phe Ser Cys Lys Cys Asp Ser Arg Ser Leu Glu Val Asp 20 25 30 Cys Ser Gly Leu Gly Leu Thr Thr Val Pro Pro Asp Val Pro Ala Ala 35 40 45 Thr Arg Thr Leu Leu Leu Leu Asn Asn Lys Leu Ser Ala Leu Pro Ser 50 55 60 Trp Ala Phe Ala Asn Leu Ser Ser Leu Gln Arg Leu Asp Leu Ser Asn 65 70 75 80 Asn Phe Leu Asp Arg Leu Pro Arg Ser Ile Phe Gly Asp Leu Thr Asn 85 90 95 Leu Thr Glu Leu Gln Leu Arg Asn Asn Ser Ile Arg Thr Leu Asp Arg 100 105 110 Asp Leu Leu Arg His Ser Pro Leu Leu Arg His Leu Asp Leu Ser Ile 115 120 125 Asn Gly Leu Ala Gln Leu Pro Pro Gly Leu Phe Asp Gly Leu Leu Ala 130 135 140 Leu Arg Ser Leu Ser Leu Arg Ser Asn Arg Leu Gln Asn Leu Asp Arg 145 150 155 160 Leu Thr Phe Glu Pro Leu Ala Asn Leu Gln Leu Leu Gln Val Gly Asp 165 170 175 Asn Pro Trp Glu Cys Asp Cys Asn Leu Arg Glu Phe Lys His Trp Met 180 185 190 Glu Trp Phe Ser Tyr Arg Gly Gly Arg Leu Asp Gln Leu Ala Cys Thr 195 200 205 Leu Pro Lys Glu Leu Arg Gly Lys Asp Met Arg Met Val Pro Met Glu 210 215 220 Met Phe Asn Tyr Cys Ser Gln Leu Glu Asp Glu Asn Ser Ser Ala Gly 225 230 235 240 Leu Asp Ile Pro Gly Pro Pro Cys Thr Lys Ala Ser Pro Glu Pro Ala 245 250 255 Lys Pro Lys Pro Gly Ala Glu Pro Glu Pro Glu Pro Ser Thr Ala Cys 260 265 270 Pro Gln Lys Gln Arg His Arg Pro Ala Ser Val Arg Arg Ala Met Gly 275 280 285 Thr Val Ile Ile Ala Gly Val Val Cys Gly Val Val Cys Ile Met Met 290 295 300 Val Val Ala Ala Ala Tyr Gly Cys Ile Tyr Ala Ser Leu Met Ala Lys 305 310 315 320 Tyr His Arg Glu Leu Lys Lys Arg Gln Pro Leu Met Gly Asp Pro Glu 325 330 335 Gly Glu His Glu Asp Gln Lys Gln Ile Ser Ser Val Ala 340 345 48 738 PRT Homo sapiens 48 Met Gly Met Thr Val Ile Lys Gln Ile Thr Asp Asp Leu Phe Val Trp 1 5 10 15 Asn Val Leu Asn Arg Glu Glu Val Asn Ile Ile Cys Cys Glu Lys Val 20 25 30 Glu Gln Asp Ala Ala Arg Gly Ile Ile His Met Ile Leu Lys Lys Gly 35 40 45 Ser Glu Ser Cys Asn Leu Phe Leu Lys Ser Leu Lys Glu Trp Asn Tyr 50 55 60 Pro Leu Phe Gln Asp Leu Asn Gly Gln Ser Leu Phe His Gln Thr Ser 65 70 75 80 Glu Gly Asp Leu Asp Asp Leu Ala Gln Asp Leu Lys Asp Leu Tyr His 85 90 95 Thr Pro Ser Phe Leu Asn Phe Tyr Pro Leu Gly Glu Asp Ile Asp Ile 100 105 110 Ile Phe Asn Leu Lys Ser Thr Phe Thr Glu Pro Val Leu Trp Arg Lys 115 120 125 Asp Gln His His His Arg Val Glu Gln Leu Thr Leu Asn Gly Leu Leu 130 135 140 Gln Ala Leu Gln Ser Pro Cys Ile Ile Glu Gly Glu Ser Gly Lys Gly 145 150 155 160 Lys Ser Thr Leu Leu Gln Arg Ile Ala Met Leu Trp Gly Ser Gly Lys 165 170 175 Cys Lys Ala Leu Thr Lys Phe Lys Phe Val Phe Phe Leu Arg Leu Ser 180 185 190 Arg Ala Gln Gly Gly Leu Phe Glu Thr Leu Cys Asp Gln Leu Leu Asp 195 200 205 Ile Pro Gly Thr Ile Arg Lys Gln Thr Phe Met Ala Met Leu Leu Lys 210 215 220 Leu Arg Gln Arg Val Leu Phe Leu Leu Asp Gly Tyr Asn Glu Phe Lys 225 230 235 240 Pro Gln Asn Cys Pro Glu Ile Glu Ala Leu Ile Lys Glu Asn His Arg 245 250 255 Phe Lys Asn Met Val Ile Val Thr Thr Thr Thr Glu Cys Leu Arg His 260 265 270 Ile Arg Gln Phe Gly Ala Leu Thr Ala Glu Val Gly Asp Met Thr Glu 275 280 285 Asp Ser Ala Gln Ala Leu Ile Arg Glu Val Leu Ile Lys Glu Leu Ala 290 295 300 Glu Gly Leu Leu Leu Gln Ile Gln Lys Ser Arg Cys Leu Arg Asn Leu 305 310 315 320 Met Lys Thr Pro Leu Phe Val Val Ile Thr Cys Ala Ile Gln Met Gly 325 330 335 Glu Ser Glu Phe His Ser His Thr Gln Thr Thr Leu Phe His Thr Phe 340 345 350 Tyr Asp Leu Leu Ile Gln Lys Asn Lys His Lys His Lys Gly Val Ala 355 360 365 Ala Ser Asp Phe Ile Arg Ser Leu Asp His Cys Gly Asp Leu Ala Leu 370 375 380 Glu Gly Val Phe Ser His Lys Phe Asp Phe Glu Leu Gln Asp Val Ser 385 390 395 400 Ser Val Asn Glu Asp Val Leu Leu Thr Thr Gly Leu Leu Cys Lys Tyr 405 410 415 Thr Ala Gln Arg Phe Lys Pro Lys Tyr Lys Phe Phe His Lys Ser Phe 420 425 430 Gln Glu Tyr Thr Ala Gly Arg Arg Leu Ser Ser Leu Leu Thr Ser His 435 440 445 Glu Pro Glu Glu Val Thr Lys Gly Asn Gly Tyr Leu Gln Lys Met Val 450 455 460 Ser Ile Ser Asp Ile Thr Ser Thr Tyr Ser Ser Leu Leu Arg Tyr Thr 465 470 475 480 Cys Gly Ser Ser Val Glu Ala Thr Arg Ala Val Met Lys His Leu Ala 485 490 495 Ala Val Tyr Gln His Gly Cys Leu Leu Gly Leu Ser Ile Ala Lys Arg 500 505 510 Pro Leu Trp Arg Gln Glu Ser Leu Gln Ser Val Lys Asn Thr Thr Glu 515 520 525 Gln Glu Ile Leu Lys Ala Ile Asn Ile Asn Ser Phe Val Glu Cys Gly 530 535 540 Ile His Leu Tyr Gln Glu Ser Thr Ser Lys Ser Ala Leu Ser Gln Glu 545 550 555 560 Phe Glu Ala Phe Phe Gln Gly Lys Ser Leu Tyr Ile Asn Ser Gly Asn 565 570 575 Ile Pro Asp Tyr Leu Phe Asp Phe Phe Glu His Leu Pro Asn Cys Ala 580 585 590 Ser Ala Leu Asp Phe Ile Lys Leu Asp Phe Tyr Gly Gly Ala Met Ala 595 600 605 Ser Trp Glu Lys Ala Ala Glu Asp Thr Gly Gly Ile His Met Glu Glu 610 615 620 Ala Pro Glu Thr Tyr Ile Pro Ser Arg Ala Val Ser Leu Phe Phe Asn 625 630 635 640 Trp Lys Gln Glu Phe Arg Thr Leu Glu Val Thr Leu Arg Asp Phe Ser 645 650 655 Lys Leu Asn Lys Gln Asp Ile Arg Tyr Leu Gly Lys Ile Phe Ser Ser 660 665 670 Ala Thr Ser Leu Arg Leu Gln Ile Lys Arg Cys Ala Gly Val Ala Gly 675 680 685 Ser Leu Ser Leu Val Leu Ser Thr Cys Lys Asn Ile Tyr Ser Leu Met 690 695 700 Val Glu Ala Ser Pro Leu Thr Ile Glu Asp Glu Arg His Ile Thr Ser 705 710 715 720 Val Thr Asn Leu Lys Thr Leu Ser Ile His Asp Leu Gln Asn Gln Arg 725 730 735 Leu Pro 49 1070 PRT Homo sapiens 49 Met Tyr Lys Ser Leu Asn Ile Asp Glu Cys Asp Leu His Ala Trp Leu 1 5 10 15 Asp Leu Pro Ala Glu Lys Pro Leu Gly Val Val Asn Arg Val Cys Trp 20 25 30 Gly Phe Ile Arg Phe Lys Gly Tyr Met Tyr Pro Leu Asp Tyr Leu Asn 35 40 45 Phe Ile Lys Asp Asn Ser Arg Ala Leu Ile Gln Arg Met Gly Met Thr 50 55 60 Val Ile Lys Gln Ile Thr Asp Asp Leu Phe Val Trp Asn Val Leu Asn 65 70 75 80 Arg Glu Glu Val Asn Ile Ile Cys Cys Glu Lys Val Glu Gln Asp Ala 85 90 95 Ala Arg Gly Ile Ile His Met Ile Leu Lys Lys Gly Ser Glu Ser Cys 100 105 110 Asn Leu Phe Leu Lys Ser Leu Lys Glu Trp Asn Tyr Pro Leu Phe Gln 115 120 125 Asp Leu Asn Gly Gln Ser Leu Phe His Gln Thr Ser Glu Gly Asp Leu 130 135 140 Asp Asp Leu Ala Gln Asp Leu Lys Asp Leu Tyr His Thr Pro Ser Phe 145 150 155 160 Leu Asn Phe Tyr Pro Leu Gly Glu Asp Ile Asp Ile Ile Phe Asn Leu 165 170 175 Lys Ser Thr Phe Thr Glu Pro Val Leu Trp Arg Lys Asp Gln His His 180 185 190 His Arg Val Glu Gln Leu Thr Leu Asn Gly Leu Leu Gln Ala Leu Gln 195 200 205 Ser Pro Cys Ile Ile Glu Gly Glu Ser Gly Lys Gly Lys Ser Thr Leu 210 215 220 Leu Gln Arg Ile Ala Met Leu Trp Gly Ser Gly Lys Cys Lys Ala Leu 225 230 235 240 Thr Lys Phe Lys Phe Val Phe Phe Leu Arg Leu Ser Arg Ala Gln Gly 245 250 255 Gly Leu Phe Glu Thr Leu Cys Asp Gln Leu Leu Asp Ile Pro Gly Thr 260 265 270 Ile Arg Lys Gln Thr Phe Met Ala Met Leu Leu Lys Leu Arg Gln Arg 275 280 285 Val Leu Phe Leu Leu Asp Gly Tyr Asn Glu Phe Lys Pro Gln Asn Cys 290 295 300 Pro Glu Ile Glu Ala Leu Ile Lys Glu Asn His Arg Phe Lys Asn Met 305 310 315 320 Val Ile Val Thr Thr Thr Thr Glu Cys Leu Arg His Ile Arg Gln Phe 325 330 335 Gly Ala Leu Thr Ala Glu Val Gly Asp Met Thr Glu Asp Ser Ala Gln 340 345 350 Ala Leu Ile Arg Glu Val Leu Ile Lys Glu Leu Ala Glu Gly Leu Leu 355 360 365 Leu Gln Ile Gln Lys Ser Arg Cys Leu Arg Asn Leu Met Lys Thr Pro 370 375 380 Leu Phe Val Val Ile Thr Cys Ala Ile Gln Met Gly Glu Ser Glu Phe 385 390 395 400 His Ser His Thr Gln Thr Thr Leu Phe His Thr Phe Tyr Asp Leu Leu 405 410 415 Ile Gln Lys Asn Lys His Lys His Lys Gly Val Ala Ala Ser Asp Phe 420 425 430 Ile Arg Ser Leu Asp His Cys Gly Asp Leu Ala Leu Glu Gly Val Phe 435 440 445 Ser His Lys Phe Asp Phe Glu Leu Gln Asp Val Ser Ser Val Asn Glu 450 455 460 Asp Val Leu Leu Thr Thr Gly Leu Leu Cys Lys Tyr Thr Ala Gln Arg 465 470 475 480 Phe Lys Pro Lys Tyr Lys Phe Phe His Lys Ser Phe Gln Glu Tyr Thr 485 490 495 Ala Gly Arg Arg Leu Ser Ser Leu Leu Thr Ser His Glu Pro Glu Glu 500 505 510 Val Thr Lys Gly Asn Gly Tyr Leu Gln Lys Met Val Ser Ile Ser Asp 515 520 525 Ile Thr Ser Thr Tyr Ser Ser Leu Leu Arg Tyr Thr Cys Gly Ser Ser 530 535 540 Val Glu Ala Thr Arg Ala Val Met Lys His Leu Ala Ala Val Tyr Gln 545 550 555 560 His Gly Cys Leu Leu Gly Leu Ser Ile Ala Lys Arg Pro Leu Trp Arg 565 570 575 Gln Glu Ser Leu Gln Ser Val Lys Asn Thr Thr Glu Gln Glu Ile Leu 580 585 590 Lys Ala Ile Asn Ile Asn Ser Phe Val Glu Cys Gly Ile His Leu Tyr 595 600 605 Gln Glu Ser Thr Ser Lys Ser Ala Leu Ser Gln Glu Phe Glu Ala Phe 610 615 620 Phe Gln Gly Lys Ser Leu Tyr Ile Asn Ser Gly Asn Ile Pro Asp Tyr 625 630 635 640 Leu Phe Asp Phe Phe Glu His Leu Pro Asn Cys Ala Ser Ala Leu Asp 645 650 655 Phe Ile Lys Leu Asp Phe Tyr Gly Gly Ala Met Ala Ser Trp Glu Lys 660 665 670 Ala Ala Glu Asp Thr Gly Gly Ile His Met Glu Glu Ala Pro Glu Thr 675 680 685 Tyr Ile Pro Ser Arg Ala Val Ser Leu Phe Phe Asn Trp Lys Gln Glu 690 695 700 Phe Arg Thr Leu Glu Val Thr Leu Arg Asp Phe Ser Lys Leu Asn Lys 705 710 715 720 Gln Asp Ile Arg Tyr Leu Gly Lys Ile Phe Ser Ser Ala Thr Ser Leu 725 730 735 Arg Leu Gln Ile Lys Arg Cys Ala Gly Val Ala Gly Ser Leu Ser Leu 740 745 750 Val Leu Ser Thr Cys Lys Asn Ile Tyr Ser Leu Met Val Glu Ala Ser 755 760 765 Pro Leu Thr Ile Glu Asp Glu Arg His Ile Thr Ser Val Thr Asn Leu 770 775 780 Lys Thr Leu Ser Ile His Asp Leu Gln Asn Gln Arg Leu Pro Gly Gly 785 790 795 800 Leu Thr Asp Ser Leu Gly Asn Leu Lys Asn Leu Thr Lys Leu Ile Met 805 810 815 Asp Asn Ile Lys Met Asn Glu Glu Asp Ala Ile Lys Leu Ala Glu Gly 820 825 830 Leu Lys Asn Leu Lys Lys Met Cys Leu Phe His Leu Thr His Leu Ser 835 840 845 Asp Ile Gly Glu Gly Met Asp Tyr Ile Val Lys Ser Leu Ser Ser Glu 850 855 860 Pro Cys Asp Leu Glu Glu Ile Gln Leu Val Ser Cys Cys Leu Ser Ala 865 870 875 880 Asn Ala Val Lys Ile Leu Ala Gln Asn Leu His Asn Leu Val Lys Leu 885 890 895 Ser Ile Leu Asp Leu Ser Glu Asn Tyr Leu Glu Lys Asp Gly Asn Glu 900 905 910 Ala Leu His Glu Leu Ile Asp Arg Met Asn Val Leu Glu Gln Leu Thr 915 920 925 Ala Leu Met Leu Pro Trp Gly Cys Asp Val Gln Gly Ser Leu Ser Ser 930 935 940 Leu Leu Lys His Leu Glu Glu Val Pro Gln Leu Val Lys Leu Gly Leu 945 950 955 960 Lys Asn Trp Arg Leu Thr Asp Thr Glu Ile Arg Ile Leu Gly Ala Phe 965 970 975 Phe Gly Lys Asn Pro Leu Lys Asn Phe Gln Gln Leu Asn Leu Ala Gly 980 985 990 Asn Arg Val Ser Ser Asp Gly Trp Leu Ala Phe Met Gly Val Phe Glu 995 1000 1005 Asn Leu Lys Gln Leu Val Phe Phe Asp Phe Ser Thr Lys Glu Phe Leu 1010 1015 1020 Pro Asp Pro Ala Leu Val Arg Lys Leu Ser Gln Val Leu Ser Lys Leu 1025 1030 1035 1040 Thr Phe Leu Gln Glu Ala Arg Leu Val Gly Trp Gln Phe Asp Asp Asp 1045 1050 1055 Asp Leu Ser Val Ile Thr Gly Ala Phe Lys Leu Val Thr Ala 1060 1065 1070 50 487 PRT Homo sapiens 50 Met Pro Pro Leu Pro Gln Trp Ser Phe Pro Arg Pro Asp His Cys His 1 5 10 15 Val Thr Phe Val Thr Leu Lys Cys Asp Ser Ser Lys Lys Arg Arg Arg 20 25 30 Gly Arg Lys Ser Pro Ser Lys Glu Val Ser His Ile Thr Ala Glu Phe 35 40 45 Glu Ile Glu Thr Lys Met Glu Glu Ala Ser Asp Thr Cys Glu Ala Asp 50 55 60 Cys Leu Arg Lys Arg Ala Glu Gln Ser Leu Gln Ala Ala Ile Lys Thr 65 70 75 80 Leu Arg Lys Ser Ile Gly Arg Gln Gln Phe Tyr Val Gln Val Ser Gly 85 90 95 Thr Glu Tyr Glu Val Ala Gln Arg Pro Ala Lys Ala Leu Glu Gly Gln 100 105 110 Gly Ala Cys Gly Ala Gly Gln Val Leu Gln Asp Ser Lys Cys Val Ala 115 120 125 Cys Gly Pro Gly Thr His Phe Gly Gly Glu Leu Gly Gln Cys Val Ser 130 135 140 Cys Met Pro Gly Thr Tyr Gln Asp Met Glu Gly Gln Leu Ser Cys Thr 145 150 155 160 Pro Cys Pro Ser Ser Asp Gly Leu Gly Leu Pro Gly Ala Arg Asn Val 165 170 175 Ser Glu Cys Gly Gly Lys Cys Gly Pro Arg Arg Arg Gly Phe Phe Ser 180 185 190 Ala Asp Gly Phe Lys Pro Cys Gln Ala Cys Pro Val Gly Thr Tyr Gln 195 200 205 Pro Glu Pro Gly Arg Thr Gly Cys Phe Pro Cys Gly Gly Gly Leu Leu 210 215 220 Thr Lys His Glu Gly Thr Thr Ser Phe Gln Asp Cys Glu Ala Lys Val 225 230 235 240 His Cys Ser Pro Gly His His Tyr Asn Thr Thr Thr His Arg Cys Ile 245 250 255 Arg Cys Pro Val Gly Thr Tyr Gln Pro Glu Phe Gly Gln Asn His Cys 260 265 270 Ile Thr Cys Pro Gly Asn Thr Ser Thr Asp Phe Asp Gly Ser Thr Asn 275 280 285 Val Thr His Cys Lys Asn Gln His Cys Gly Gly Glu Leu Gly Asp Tyr 290 295 300 Thr Gly Tyr Ile Glu Ser Pro Asn Tyr Pro Gly Asp Tyr Pro Ala Asn 305 310 315 320 Ala Glu Cys Val Trp His Ile Ala Pro Pro Pro Lys Arg Arg Ile Leu 325 330 335 Ile Val Val Pro Glu Ile Phe Leu Pro Ile Glu Asp Glu Cys Gly Asp 340 345 350 Val Leu Val Met Arg Lys Ser Ala Ser Pro Thr Ser Ile Thr Thr Tyr 355 360 365 Glu Thr Cys Gln Thr Tyr Glu Arg Pro Ile Ala Phe Thr Ser Arg Ser 370 375 380 Arg Lys Leu Trp Ile Gln Phe Lys Ser Asn Glu Gly Asn Ser Gly Lys 385 390 395 400 Gly Phe Gln Val Pro Tyr Val Thr Tyr Asp Glu Asp Tyr Gln Gln Leu 405 410 415 Ile Glu Asp Ile Val Arg Asp Gly Arg Leu Tyr Ala Ser Glu Asn His 420 425 430 Gln Glu Ile Leu Lys Asp Lys Lys Leu Ile Lys Ala Leu Phe Asp Val 435 440 445 Leu Ala His Pro Gln Asn Tyr Phe Lys Tyr Thr Ala Gln Glu Ser Lys 450 455 460 Glu Met Phe Pro Arg Ser Phe Ile Lys Leu Leu Arg Ser Lys Val Ser 465 470 475 480 Arg Phe Leu Arg Pro Tyr Lys 485 51 965 PRT Homo sapiens 51 Met Gly Ala Ala Ala Val Arg Trp His Leu Cys Val Leu Leu Ala Leu 1 5 10 15 Gly Thr Arg Gly Arg Leu Ala Gly Gly Ser Gly Leu Pro Gly Ser Val 20 25 30 Asp Val Asp Glu Cys Ser Glu Gly Thr Asp Asp Cys His Ile Asp Ala 35 40 45 Ile Cys Gln Asn Thr Pro Lys Ser Tyr Lys Cys Leu Cys Lys Pro Gly 50 55 60 Tyr Lys Gly Glu Gly Lys Gln Cys Glu Asp Ile Asp Glu Cys Glu Asn 65 70 75 80 Asp Tyr Tyr Asn Gly Gly Cys Val His Glu Cys Ile Asn Ile Pro Gly 85 90 95 Asn Tyr Arg Cys Thr Cys Phe Asp Gly Phe Met Leu Ala His Asp Gly 100 105 110 His Asn Cys Leu Asp Val Asp Glu Cys Gln Asp Asn Asn Gly Gly Cys 115 120 125 Gln Gln Ile Cys Val Asn Ala Met Gly Ser Tyr Glu Cys Gln Cys His 130 135 140 Ser Gly Phe Phe Leu Ser Asp Asn Gln His Thr Cys Ile His Arg Ser 145 150 155 160 Asn Glu Gly Met Asn Cys Met Asn Lys Asp His Gly Cys Ala His Ile 165 170 175 Cys Arg Glu Thr Pro Lys Gly Gly Val Ala Cys Asp Cys Arg Pro Gly 180 185 190 Phe Asp Leu Ala Gln Asn Gln Lys Asp Cys Thr Leu Thr Cys Asn Tyr 195 200 205 Gly Asn Gly Gly Cys Gln His Ser Cys Glu Asp Thr Asp Thr Gly Pro 210 215 220 Thr Cys Gly Cys His Gln Lys Tyr Ala Leu His Ser Asp Gly Arg Thr 225 230 235 240 Cys Ile Glu Thr Cys Ala Val Asn Asn Gly Gly Cys Asp Arg Thr Cys 245 250 255 Lys Asp Thr Ala Thr Gly Val Arg Cys Ser Cys Pro Val Gly Phe Thr 260 265 270 Leu Gln Pro Asp Gly Lys Thr Cys Lys Asp Ile Asn Glu Cys Leu Val 275 280 285 Asn Asn Gly Gly Cys Asp His Phe Cys Arg Asn Thr Val Gly Ser Phe 290 295 300 Glu Cys Gly Cys Arg Lys Gly Tyr Lys Leu Leu Thr Asp Glu Arg Thr 305 310 315 320 Cys Gln Asp Ile Asp Glu Cys Ser Phe Glu Arg Thr Cys Asp His Ile 325 330 335 Cys Ile Asn Ser Pro Gly Ser Phe Gln Cys Leu Cys His Arg Gly Tyr 340 345 350 Ile Leu Tyr Gly Thr Thr His Cys Gly Asp Val Asp Glu Cys Ser Met 355 360 365 Ser Asn Gly Ser Cys Asp Gln Gly Cys Val Asn Thr Lys Gly Ser Tyr 370 375 380 Glu Cys Val Cys Pro Pro Gly Arg Arg Leu His Trp Asn Gly Lys Asp 385 390 395 400 Cys Val Glu Thr Gly Lys Cys Leu Ser Arg Ala Lys Thr Ser Pro Arg 405 410 415 Ala Gln Leu Ser Cys Ser Lys Ala Gly Gly Val Glu Ser Cys Phe Leu 420 425 430 Ser Cys Pro Ala His Thr Leu Phe Val Pro Asp Ser Glu Asn Ser Tyr 435 440 445 Val Leu Ser Cys Gly Val Pro Gly Pro Gln Gly Lys Ala Leu Gln Lys 450 455 460 Arg Asn Gly Thr Ser Ser Gly Leu Gly Pro Ser Cys Ser Asp Ala Pro 465 470 475 480 Thr Thr Pro Ile Lys Gln Lys Ala Arg Phe Lys Ile Arg Asp Ala Lys 485 490 495 Cys His Leu Arg Pro His Ser Gln Ala Arg Ala Lys Glu Thr Ala Arg 500 505 510 Gln Pro Leu Leu Asp His Cys His Val Thr Phe Val Thr Leu Lys Cys 515 520 525 Asp Ser Ser Lys Lys Arg Arg Arg Gly Arg Lys Ser Pro Ser Lys Glu 530 535 540 Val Ser His Ile Thr Ala Glu Phe Glu Ile Glu Thr Lys Met Glu Glu 545 550 555 560 Ala Ser Asp Thr Cys Glu Ala Asp Cys Leu Arg Lys Arg Ala Glu Gln 565 570 575 Ser Leu Gln Ala Ala Ile Lys Thr Leu Arg Lys Ser Ile Gly Arg Gln 580 585 590 Gln Phe Tyr Val Gln Val Ser Gly Thr Glu Tyr Glu Val Ala Gln Arg 595 600 605 Pro Ala Lys Ala Leu Glu Gly Gln Gly Ala Cys Gly Ala Gly Gln Val 610 615 620 Leu Gln Asp Ser Lys Cys Val Ala Cys Gly Pro Gly Thr His Phe Gly 625 630 635 640 Gly Glu Leu Gly Gln Cys Val Ser Cys Met Pro Gly Thr Tyr Gln Asp 645 650 655 Met Glu Gly Gln Leu Ser Cys Thr Pro Cys Pro Ser Ser Asp Gly Leu 660 665 670 Gly Leu Pro Gly Ala Arg Asn Val Ser Glu Cys Gly Gly Gln Cys Ser 675 680 685 Pro Gly Phe Phe Ser Ala Asp Gly Phe Lys Pro Cys Gln Ala Cys Pro 690 695 700 Val Gly Thr Tyr Gln Pro Glu Pro Gly Arg Thr Gly Cys Phe Pro Cys 705 710 715 720 Gly Gly Gly Leu Leu Thr Lys His Glu Gly Thr Thr Ser Phe Gln Asp 725 730 735 Cys Glu Ala Lys Val His Cys Ser Pro Gly His His Tyr Asn Thr Thr 740 745 750 Thr His Arg Cys Ile Arg Cys Pro Val Gly Thr Tyr Gln Pro Glu Phe 755 760 765 Gly Gln Asn His Cys Ile Thr Cys Pro Gly Asn Thr Ser Thr Asp Phe 770 775 780 Asp Gly Ser Thr Asn Val Thr His Cys Lys Asn Gln His Cys Gly Gly 785 790 795 800 Glu Leu Gly Asp Tyr Thr Gly Tyr Ile Glu Ser Pro Asn Tyr Pro Gly 805 810 815 Asp Tyr Pro Ala Asn Ala Glu Cys Val Trp His Ile Ala Pro Pro Pro 820 825 830 Lys Arg Arg Ile Leu Ile Val Val Pro Glu Ile Phe Leu Pro Ile Glu 835 840 845 Asp Glu Cys Gly Asp Val Leu Val Met Arg Lys Ser Ala Ser Pro Thr 850 855 860 Ser Ile Thr Thr Tyr Glu Thr Cys Gln Thr Tyr Glu Arg Pro Ile Ala 865 870 875 880 Phe Thr Ser Arg Ser Arg Lys Leu Trp Ile Gln Phe Lys Ser Asn Glu 885 890 895 Gly Asn Ser Gly Lys Gly Phe Gln Val Pro Tyr Val Thr Tyr Asp Gly 900 905 910 Lys Ile His Cys Leu His Gly Pro Leu Cys Thr Ala Gln Ala Gly Pro 915 920 925 Trp Arg His Arg Asp Glu Ser His Val Pro Ala Pro Ser Gly Ser Cys 930 935 940 Asp Leu Ala Gly Thr Asp Leu Glu Ala Glu Arg Thr Leu Ser Gly Ala 945 950 955 960 Arg Ala Arg Gln Ala 965 52 716 PRT Homo sapiens 52 Met Ala Arg Met Ser Phe Val Ile Ala Ala Cys Gln Leu Val Leu Gly 1 5 10 15 Leu Leu Met Thr Ser Leu Thr Glu Ser Ser Ile Gln Asn Ser Glu Cys 20 25 30 Pro Gln Leu Cys Val Cys Glu Ile Arg Pro Trp Phe Thr Pro Gln Ser 35 40 45 Thr Tyr Arg Glu Ala Thr Thr Val Asp Cys Asn Asp Leu Arg Leu Thr 50 55 60 Arg Ile Pro Ser Asn Leu Ser Ser Asp Thr Gln Val Leu Leu Leu Gln 65 70 75 80 Ser Asn Asn Ile Ala Lys Thr Val Asp Glu Leu Gln Gln Leu Phe Asn 85 90 95 Leu Thr Glu Leu Asp Phe Ser Gln Asn Asn Phe Thr Asn Ile Lys Glu 100 105 110 Val Gly Leu Ala Asn Leu Thr Gln Leu Thr Thr Leu His Leu Glu Glu 115 120 125 Asn Gln Ile Thr Glu Met Thr Asp Tyr Cys Leu Gln Asp Leu Ser Asn 130 135 140 Leu Gln Glu Leu Tyr Ile Asn His Asn Gln Ile Ser Thr Ile Ser Ala 145 150 155 160 His Ala Phe Ala Gly Leu Lys Asn Leu Leu Arg Leu His Leu Asn Ser 165 170 175 Asn Lys Leu Lys Val Ile Asp Ser Arg Trp Phe Asp Ser Thr Pro Asn 180 185 190 Leu Glu Ile Leu Met Ile Gly Glu Asn Pro Val Ile Gly Ile Leu Asp 195 200 205 Met Asn Phe Lys Pro Leu Ala Asn Leu Arg Ser Leu Val Leu Ala Gly 210 215 220 Met Tyr Leu Thr Asp Ile Pro Gly Asn Ala Leu Val Gly Leu Asp Ser 225 230 235 240 Leu Glu Ser Leu Ser Phe Tyr Asp Asn Lys Leu Val Lys Val Pro Gln 245 250 255 Leu Ala Leu Gln Lys Val Pro Asn Leu Lys Phe Leu Asp Leu Asn Lys 260 265 270 Asn Pro Ile His Lys Ile Gln Glu Gly Asp Phe Lys Asn Met Leu Arg 275 280 285 Leu Lys Glu Leu Gly Ile Asn Asn Met Gly Glu Leu Val Ser Val Asp 290 295 300 Arg Tyr Ala Leu Asp Asn Leu Pro Glu Leu Thr Lys Leu Glu Ala Thr 305 310 315 320 Asn Asn Pro Lys Leu Ser Tyr Ile His Arg Leu Ala Phe Arg Ser Val 325 330 335 Pro Ala Leu Glu Ser Leu Met Leu Asn Asn Asn Ala Leu Asn Ala Ile 340 345 350 Tyr Gln Lys Thr Val Glu Ser Leu Pro Asn Leu Arg Glu Ile Ser Ile 355 360 365 His Ser Asn Pro Leu Arg Cys Asp Cys Val Ile His Trp Ile Asn Ser 370 375 380 Asn Lys Thr Asn Ile Arg Phe Met Glu Pro Leu Ser Met Phe Cys Ala 385 390 395 400 Met Pro Pro Glu Tyr Lys Gly His Gln Val Lys Glu Val Leu Ile Gln 405 410 415 Asp Ser Ser Glu Gln Cys Leu Pro Met Ile Ser His Asp Ser Phe Pro 420 425 430 Asn Arg Leu Asn Val Asp Ile Gly Thr Thr Val Phe Leu Asp Cys Arg 435 440 445 Ala Met Ala Glu Pro Glu Pro Glu Ile Tyr Trp Val Thr Pro Ile Gly 450 455 460 Asn Lys Ile Thr Val Glu Thr Leu Ser Asp Lys Tyr Lys Leu Ser Ser 465 470 475 480 Glu Gly Thr Leu Glu Ile Ser Asn Ile Gln Ile Glu Asp Ser Gly Arg 485 490 495 Tyr Thr Cys Val Ala Gln Asn Val Gln Gly Ala Asp Thr Arg Val Ala 500 505 510 Thr Ile Lys Val Asn Gly Thr Leu Leu Asp Gly Thr Gln Val Leu Lys 515 520 525 Ile Tyr Val Lys Gln Thr Glu Ser His Ser Ile Leu Val Ser Trp Lys 530 535 540 Val Asn Ser Asn Val Met Thr Ser Asn Leu Lys Trp Ser Ser Ala Thr 545 550 555 560 Met Lys Ile Asp Asn Pro His Ile Thr Tyr Thr Ala Arg Val Pro Val 565 570 575 Asp Val His Glu Tyr Asn Leu Thr His Leu Gln Pro Ser Thr Asp Tyr 580 585 590 Glu Val Cys Leu Thr Val Ser Asn Ile His Gln Gln Thr Gln Lys Ser 595 600 605 Cys Val Asn Val Thr Thr Lys Asn Ala Ala Phe Ala Val Asp Ile Ser 610 615 620 Asp Gln Glu Thr Ser Thr Ala Leu Ala Ala Val Met Gly Ser Met Phe 625 630 635 640 Ala Val Ile Ser Leu Ala Ser Ile Ala Val Tyr Phe Ala Lys Arg Phe 645 650 655 Lys Arg Lys Asn Tyr His His Ser Leu Lys Lys Tyr Met Gln Lys Thr 660 665 670 Ser Ser Ile Pro Leu Asn Glu Leu Tyr Pro Pro Leu Ile Asn Leu Trp 675 680 685 Glu Gly Asp Ser Glu Lys Asp Lys Asp Gly Ser Ala Asp Thr Lys Pro 690 695 700 Thr Gln Val Asp Thr Ser Arg Ser Tyr Tyr Met Trp 705 710 715 

What is claimed is:
 1. An isolated polypeptide selected from the group consisting of: (a) an isolated polypeptide encoded by a polynucleotide comprising a sequence set forth in Table I; (b) an isolated polypeptide comprising a polypeptide sequence set forth in Table I; and (c) a polypeptide sequence of a gene set forth in Table I.
 2. An isolated polynucleotide selected from the group consisting of: (a) an isolated polynucleotide comprising a polynucleotide sequence set forth in Table I; (b) an isolated polynucleotide of a gene set forth in Table I; (c) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide set forth in Table I; (d) an isolated polynucleotide encoding a polypeptide set forth in Table I; (e) a polynucleotide which is an RNA equivalent of the polynucleotide of (a) to (d); or a polynucleotide sequence complementary to said isolated polynucleotide.
 3. An expression vector comprising a polynucleotide capable of producing a polypeptide of claim 1 when said expression vector is present in a compatible host cell.
 4. A process for producing a recombinant host cell which comprises the step of introducing an expression vector comprising a polynucleotide capable of producing a polypeptide of claim 1 into a cell such that the host cell, under appropriate culture conditions, produces said polypeptide.
 5. A recombinant host cell produced by the process of claim
 6. 6. A membrane of a recombinant host cell of claim 7 expressing said polypeptide.
 7. A process for producing a polypeptide which comprises culturing a host cell of claim 7 under conditions sufficient for the production of said polypeptide and recovering said polypeptide from the culture. 